EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-11642 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr18:74764740-74769660 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs180931486chr1874767541hg19
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ATF3MA0605.2chr18:74766744-74766756GGTGACGTCACC+6.22
ATF3MA0605.2chr18:74766744-74766756GGTGACGTCACC-6.22
CREB1MA0018.3chr18:74766744-74766756GGTGACGTCACC+7.22
CREB1MA0018.3chr18:74766744-74766756GGTGACGTCACC-7.22
EWSR1-FLI1MA0149.1chr18:74767510-74767528TCATCCTTCCTTCCTTTT-6.06
EWSR1-FLI1MA0149.1chr18:74767464-74767482CTTTCCTTCCTTTCCTTC-6.42
EWSR1-FLI1MA0149.1chr18:74767506-74767524CTTTTCATCCTTCCTTCC-6.95
EWSR1-FLI1MA0149.1chr18:74767460-74767478CTTTCTTTCCTTCCTTTC-7.36
IRF1MA0050.2chr18:74767491-74767512CCTTTCTTTCCCTTTCTTTTC+6.3
IRF1MA0050.2chr18:74767523-74767544CTTTTCTTTCTCTTTCTTTCT+6.95
Klf12MA0742.1chr18:74768897-74768912GACCACGCCCACACC+6.3
Klf1MA0493.1chr18:74766344-74766355AGCCACACCCA+6.14
MecomMA0029.1chr18:74769283-74769297CAGACAAGATAATC+6.02
SP1MA0079.4chr18:74768895-74768910CTGACCACGCCCACA+6.53
SP3MA0746.2chr18:74768897-74768910GACCACGCCCACA+6.21
SP4MA0685.1chr18:74768895-74768912CTGACCACGCCCACACC+6.47
SPI1MA0080.4chr18:74764970-74764984AAAAAGGGGAACTT+6.2
ZEB1MA0103.3chr18:74766219-74766230CCCACCTGCGC+6.62
ZNF263MA0528.1chr18:74767498-74767519TTCCCTTTCTTTTCATCCTTC-6.38
Number of super-enhancer constituents: 48             
IDCoordinateTissue/cell
SE_02301chr18:74765615-74769291Astrocytes
SE_03187chr18:74763012-74767105Brain_Angular_Gyrus
SE_03187chr18:74767106-74767924Brain_Angular_Gyrus
SE_03187chr18:74768362-74769202Brain_Angular_Gyrus
SE_03925chr18:74762993-74769676Brain_Anterior_Caudate
SE_04802chr18:74760877-74769887Brain_Cingulate_Gyrus
SE_05798chr18:74762601-74769949Brain_Hippocampus_Middle
SE_06694chr18:74761722-74769901Brain_Hippocampus_Middle_150
SE_07751chr18:74762635-74769942Brain_Inferior_Temporal_Lobe
SE_09139chr18:74763390-74771272CD14
SE_10547chr18:74764261-74769635CD19_Primary
SE_11015chr18:74762704-74785115CD20
SE_12115chr18:74764048-74769337CD3
SE_13103chr18:74764172-74765346CD34_Primary_RO01480
SE_13103chr18:74765655-74769275CD34_Primary_RO01480
SE_13673chr18:74763883-74769625CD34_Primary_RO01536
SE_14260chr18:74763782-74769393CD34_Primary_RO01549
SE_15038chr18:74763788-74768613CD4_Memory_Primary_7pool
SE_15651chr18:74764917-74768462CD4_Memory_Primary_8pool
SE_16468chr18:74765452-74768807CD4_Naive_Primary_8pool
SE_17255chr18:74765526-74769066CD4p_CD225int_CD127p_Tmem
SE_17959chr18:74762819-74769776CD4p_CD25-_CD45ROp_Memory
SE_18700chr18:74763026-74769998CD4p_CD25-_Il17-_PMAstim_Th
SE_19374chr18:74763980-74769767CD4p_CD25-_Il17p_PMAstim_Th17
SE_19981chr18:74763553-74769915CD56
SE_21261chr18:74765053-74769077CD8_Memory_7pool
SE_22307chr18:74763553-74769856CD8_primiary
SE_25341chr18:74763020-74769931DND41
SE_25885chr18:74765504-74769852Duodenum_Smooth_Muscle
SE_26884chr18:74764538-74766920Esophagus
SE_26884chr18:74767691-74769645Esophagus
SE_30168chr18:74765890-74769751Fetal_Muscle
SE_34994chr18:74765147-74769503HeLa
SE_39197chr18:74765915-74769297IMR90
SE_41189chr18:74765691-74769624Left_Ventricle
SE_42218chr18:74764253-74769817Lung
SE_47137chr18:74764303-74771360Panc1
SE_48227chr18:74765445-74769622Psoas_Muscle
SE_49182chr18:74765702-74767536Right_Atrium
SE_49182chr18:74767754-74769611Right_Atrium
SE_50626chr18:74764327-74769788Sigmoid_Colon
SE_51089chr18:74763882-74771359Skeletal_Muscle
SE_52417chr18:74764263-74769800Small_Intestine
SE_53332chr18:74764213-74769843Spleen
SE_58547chr18:74756065-74865317Ly1
SE_61817chr18:74764079-74793826Toledo
SE_62620chr18:74763866-74793718Tonsil
SE_65574chr18:74763757-74769532Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 6             
ChromosomeStartEnd
chr187476490274765159
chr187476600074769347
chr187476660274767022
chr187476703374767545
chr187476759174768136
chr187476865574769369
Number: 1             
IDChromosomeStartEnd
GH18I077051chr187476336674770955
Enhancer Sequence
GCCAGCCCAG CAACACCGGG CCTGAGTCCC CGAGCCCCCA CTCCTCTCCA CTCAGCAGGG 60
GCCCCCTCAC GCCATGTATA CCCCCCGGGT GGACTTCAGG GGCGCTGTCC CTGTGGGCGC 120
TGTGCCCTTG CCGTCCTAAC CTACTCCCTC CTGTGGAGCC ACTGGCAAGG TTTTGGGGAA 180
CATGGGTGTG AGTCCACGCT AGACCTCAGC TGCCTGCCCT GGATCATTTG AAAAAGGGGA 240
ACTTTTAGTT TCCTGCTAAA TAGAAGGCCC CAAAAGAAGC CAACCAATGC CGTGTCCCCG 300
TGATAGGCCA GCGTGGCTGT CCCAGAAGCA GAGAGGGGAA CAGCACAGGC TCGCATGTCT 360
CCAGGGAGCT CAACACCAGA TGGCTTAGTG ATAGGAGCCC TGGCTGAGGG TGGCCGCATC 420
TGCAGTGACA TGGCTGCTTC CCACTTCCCT GCACCTGTCC TCATGGTGGC TGCTTCAGGG 480
GAGGGGTGGG CAGGGGCCCC ACTGCAGGTC CAGCCAAGGG GCACACAGAA GCTGGACATT 540
TGCACACTCA GCTGGGTCGG GACTGAGCTC CGTCCTCAGC CCCTGCAGCC AAGACGCCAG 600
TGTCAGCCGG TATGCTCCGC TACGGGGGCT GGCTGTGGTT TCAGAGTCTC ACCCTAATTC 660
CAAAGAACAA AAGCATCTCT CGAGTTCCAG GGACATTTTG TCAGTTGGAA CAGCATTTCT 720
ATAGTGTGCA CCCCACATGC TATGTGCACA CATCACAAAG CACACACGGG TACTCTTACA 780
CACACACACT CTGATGCACG AGCTGCGGGC ACTTCTGTGC ATCACTTGCT GAGCTGTAGC 840
ATAGAGGCAG AATTCCTTAC AGGGAAGAGT TCAGGCCTCA GGCACACTGT CTGCTGGCAT 900
TTTATGTGGA ACACTGCCAT GTGCAAATGA AGTCTTTGAG ACAGGAGAGG AGAGAGCAGC 960
AGGGACGAGG GGTGTCCCAC CTGTCACTCA GTCATCCAGC AAATATTGAT GAAGCTCGTC 1020
CCATGAGCCG GGCCTGCGTC TAGGTGCTGG GATATCTCAG CGAACAAAAC AGACAGATGT 1080
CCCTGCCTTC ATGGGGCTCA CTTTCCATCC GGAGTCGGGG CTCGGACAAT AAACAACATA 1140
ATCAGGGACT GTGACAGAGG TGACTGTACT GCCCCACTCT GCATCCTTCT TCCTCTTGGC 1200
CCCCTCCTCG AGGTGGGGCC ACATGATGCT TCTGGCCATC AGAACTTGAG TGGACGCGAT 1260
GACTGCCCCT CGGCCTGGTC TGCAGGGTGC TTGGCCCTTG GGCTGTCCTC CCGGTCCCTC 1320
CCCGCCCTGC CCTCCGATGG CAGAGACTCT ATGTGGAAGC CACAGGACTC TCCCAGGCAC 1380
ACTGGATGGA GAGCCGCCTG GCCCTCGCTG AGCTATGATG TGAGTGGACA TCACCTTGAG 1440
CCTCAGAGAT TTAGGAGTTC CTCTGGCAGG CCTGCAGAGC CCACCTGCGC TGACACAGCT 1500
GCACTTCTAA GTGGGAGATG TCAACGAGAA GGGACATGGA GCGAAGAGCT CACCCCCGGA 1560
TATCTGGGCA AGAGACTTAA GGAGGAGGGC AGAGCTTGTG CTTCAGCCAC ACCCAGGAGG 1620
CTGCGGGAGG GAGGGGCCGC AGGAGATGTG GTTGGAGAGG CCCCTGGGGA ACAGGTGGAG 1680
GGGATTTGAG CAGGGAGCGA GGTGCTCAGC AGCTAGCTGG CAGGGAGAAC CAACAGGGAT 1740
GGATCAGGAT GGAGGCTGGG ACCCACTTAA TCACCCAGGT GGGCAGAGGA GGGCTTGGGC 1800
CTTGGTGATG GGAGAGGTGC TTGCTAAGTA TCAGAGCTTC CCTGGGTCCT TGGCACAATC 1860
AGCCATCAGT GCTCTCAGCA AAGACATAGA AATAGTGCTC CTCATTTTGT ACCTGGATAA 1920
GGGGAGAGCT CAAGTTCCAA TCCCTGTTAG CGGCGGGTGA CACAACCATG CACACATCTC 1980
AAATTCCAAT TCCTGTTAGC GGCGGGTGAC GTCACCATGC ACACATCTCA AGTTCCAGTT 2040
CCTGTTAGCG GTGGGTAATG TCACCATGCA CACATCCTGT TTTCTCCTGC TCTGCCACTG 2100
TGATCTCCAG ATGATCAATT TCATATTATC AGGAAAATGA CCTTTGGCAC AGAAAGCCCA 2160
GAGGAGAAGG TGAGGGACTT GCATGCACGC ACACATTTAA ATGTCAACAT TCTATGGAAT 2220
TCAGTATCAT AAAGGTATGC AAACCATGGG AAGTAATCAT GAGTTTGCTC TGGGAGGCCC 2280
CGCAGTTAGA AGGGAACCTT CTGGGCACGC ACATCGTGGA TGGAGACAGA GGAACGGCAG 2340
CGCCGCCTGC TGCTGCTGGG CCCTGCGTGT CTGTACCACC TTCTGTGGTA GAGAAAACAG 2400
CAGGCGGCTT TGCTGCAAAC TCCAGCACAG CCTCTGTGTG GGAGGAGCAG GGTCAGCAGA 2460
AACCCAGAGG CAGGAAGGAG CTGAGCTGAG CTGGTGCAAG AGTGTCCTGC CCTGGGAGGA 2520
AGTGGCTTTG TACCAACTGA TAAAATGCCC AGAGTAGGGG GCACATAACT GTAAACTTCT 2580
AGAACCCACA TCCTCAAAGC CCAACCCCTG ACCCAGGAGG TGCATGGGTG GCTGTTCCCT 2640
CCCAGCCCAG TGCCACCTCT GCCATCCTCC CTGGCTGGGA AAGATGAACT GCGCTTAAAA 2700
TGGGCTCAGT TTTCTTTTTC CTTTCTTTCC TTCCTTTCCT TCCATTCCTT CCCTTTCTTT 2760
CCCTTTCTTT TCATCCTTCC TTCCTTTTCT TTCTCTTTCT TTCTCTCTCT CTCTCTCTTT 2820
CTTTCTCTTT TTTTAACCTA GTAATTGCTT TTCACATCTG CTGGTGGGCT GCTATCTTTC 2880
ATAGGATAAC TTCCATTATT GCTTTAAATA AGGTGGTGTT TGGCCTCTGT TTTGTTTTCA 2940
GGTAAAGCAA ACTGCAATCA GGAAGCCCTC ATTACAGACA GTGAGGTCAT GACAAGAAAA 3000
GTTCATTCAC ACTGGAGAGT TCAACCCCAT TGGAAATGTC TTTCCAAACA CAGCTGGTGA 3060
CTTTGCAAAC CCAGACATTC CCAGAAACTC AGTGGTTCTA GAAACTTGCT TGGAATAATT 3120
AAGGTTTTAG AGCAGCTGTT GGAATTTTTA GAAAGGAAAA AAAGAAAAAA CGAAGTGAGG 3180
CTCCCCCTCC CCGACTCCTC TTACACATCC CTGTGGCTCT GTGGTGTCAC GGCTGAGCGT 3240
GCTGCGCTCC ACTGACCGTG TGGATGAAGG GCAGGCAGCA CCTGGGTGCA TTTGTGCCAG 3300
CGCATGGCAG TGAGGCCGCT GGCAGTGCAT TTCCTGTTAT CCGTGACCCC GTGCGCCCGG 3360
GGCTGGGTCT GCAGAGGCTT TGGGGAACAC ACTGTTGCTG TCTCCTGTGC CTGGCCCGGT 3420
GTCCATGTGG CTCACAGGAC CCATAGGGAC CAGGTGCTGC TCTAAACTGG AGGCATGAAC 3480
TGACCATTGG CCCAGACAGC CTTGCCATTC CCGTCCGGGG GATTAAACCT TGAACAGGTT 3540
TTGTAGGACT CTCAGCCCCA ACTTCCTTGT CTCTAGAAAA CTTGCCACTA TGAATTATTT 3600
CTCCGTCCCT TTGAGACATC GGCCCTTTCC TGGCCTCTTG CTCAGTTCAC TGCCCAGCTT 3660
TGTCTTCTCG AAGGACCCAG GAGCCTTTGA AATGTAACCA ACAAGGAAGA TAACACCCTC 3720
AGCTCCCAGT CCCTGCGGGA GGCAGGGGCC TAACTGTGGT AAGCGCTAAT CTGCAAACAT 3780
TGCTGGCCTG ACTGCACCAA CCGGCCTCCA TCCGATGTCC TCCAGGACTC TCCCACCAGC 3840
TCACCCCAGT GCTTAAAAAC CCTCCCGCCT TTCGTTTCAG CAGGGTGGAG TTCAGCTCGC 3900
TCTCTCCTAC TGCAATAGTC TGGGATACGT CTTCCCTGCC TGTCTCACTC TCCCTGGGGT 3960
AACTTTTCTT TGACACCACT GAGTCCTCCC AGCAACCTGC AGCTGAGCAC ACAACCCCCC 4020
TCTGCACAGG GGAACCGAGT CCACAGTCCT AACTACCAAA TGACATGGCC TCACTAAAGT 4080
AACTCCTAGA AGCCGAGACC TTTGTCCGAC AGCTCTCAGG AGAGGCTGCC GAGGAGAACC 4140
GGCTTCCCAC GTGCCCTGAC CACGCCCACA CCCACGGCGT GAGATTTCAC CACTCAGCCG 4200
CTGAGAAGCA GGGGGTCTTT GGCCCAAAAC AAACATCCTC TGAGACGGGA AGGAGGCATG 4260
TCCCCCAAGA ACTGCCTGGG TACTACAATG AAGCAGGGTA AATATTCAGA AGTGTGTTTG 4320
GGTTTTTAAT GATATAAAGT ATCATTAACA TTCACTTCAA CGCACAGAGG AGAAGTAACT 4380
GTTACAGTGT TTGTTTTCAC ATCTGTCAGA CAGACATGAG AACTGCCCTG CCCCTCAAGG 4440
AACCAGCTGC GGTCTCCCTG GCTGGCTGGG AGCACTGGGC TCCGATCCTG CTCCTGAGTG 4500
TCTGCCTGGC AGCTGCACCC TCATCTGACA TGCAAGGCGG GGTCAGACAA GATAATCTGA 4560
ATATTCCTTC ATCCCCCAAC TTGTGATTTT GTTTCTATGA TTTATACCCA GCCCAAAGAT 4620
GCTATTTCAC AAAATGGGTT TTGTGGCTTG TCTAGACAGG AATACAAGGC CTCAGGCAGC 4680
CACGGAATCA CAATTAGCGA TCCATTCACA CTAGCACCGA ATATTCCCAC GGAAAGGCCG 4740
TGCAGTGATT ATCTCTAAGG ACAAGGACTG TGTGTGAAGA AGGACAAGGA GAGAGGAGCT 4800
CCCGCGACTG CCAGGTCCAA ATGGAATTTT ACATCGGAAA TGACAGCTAC TTACTAAAGT 4860
CTTGTAGCTT AGTTTACTAA CCTGGATGCA TTAAATACAC ACATCATTTG AAAAATAGCA 4920