EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS082-03438 
Organism
Homo sapiens 
Tissue/cell
HCASMC 
Coordinate
chr1:235146400-235149680 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs57941271chr1235149261hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr1:235147328-235147348CCCCCACACACACCCACGCC+6.07
ZNF263MA0528.1chr1:235147070-235147091TTTTCCTCTCTCACCTCCCCC-6.41
ZNF263MA0528.1chr1:235148891-235148912GAAGAAGGGCGGGGGAGAGGA+6.65
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_02305chr1:235147035-235148901Astrocytes
SE_06052chr1:235147258-235149727Brain_Hippocampus_Middle
SE_25800chr1:235146945-235149402Duodenum_Smooth_Muscle
SE_26806chr1:235147079-235148893Esophagus
SE_29689chr1:235147728-235149217Fetal_Muscle
SE_31235chr1:235146510-235149391Fetal_Thymus
SE_32614chr1:235140175-235154143GM12878
SE_33758chr1:235147075-235148879HCC1954
SE_34767chr1:235147005-235148891HeLa
SE_36058chr1:235146614-235149471HMEC
SE_36952chr1:235146938-235152568HSMMtube
SE_37966chr1:235146872-235149155HUVEC
SE_40653chr1:235147027-235149414Left_Ventricle
SE_42265chr1:235147105-235148992Lung
SE_44202chr1:235146927-235148930NHDF-Ad
SE_45558chr1:235146593-235149758Osteoblasts
SE_47119chr1:235148155-235149767Panc1
SE_50071chr1:235146899-235149198Sigmoid_Colon
SE_51271chr1:235147542-235149156Skeletal_Muscle
SE_52352chr1:235147001-235149055Small_Intestine
SE_53330chr1:235146848-235149167Spleen
SE_56068chr1:235146597-235149251u87
SE_57395chr1:235146972-235147669VACO_503
SE_59274chr1:235138265-235187641Ly3
SE_60969chr1:235059965-235155853HBL1
SE_62329chr1:235047040-235185428Tonsil
SE_63542chr1:235146861-235147654HSMM
SE_63542chr1:235147688-235148831HSMM
SE_65393chr1:235146807-235149156Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1235146978235147112
chr1235148474235149499
Number: 1             
IDChromosomeStartEnd
GH01I235010chr1235145789235150146
Enhancer Sequence
CACTGCAAAC TCCGTCTCTG GGTTTCAAGT GATTCTCCTG CCTCAGCCTC CCGAGTAGCT 60
GGGATTACAG GTGCCCGCCA CCATGCCTGG CTAATTTTTG TATTTTTAGT AGAGACAGGG 120
TTTCACCATG TTAGCCAGAC TGGTCTCAAA ACTCCTGACC TCAAGTGATC AGCCCGCCTC 180
CGCCACCCAA AGTGCTGGGA TTACACGTGT CAGCCACCGT GCCTGGCCTC CATCGTAACC 240
ATTTTTAAGC ACGTTGTTCA GTGGTGTGAC ATGCATTCCC ACTGCTATAC AGCCATCGCC 300
GCTAACCATC TCCAGGCACT TTCATCTTGT AAAATTGAAA CTCTGCACCC ATTCAACAAT 360
AACTCCCCAC GTCCCATTCC CCTCAACTAT ATCTTTTTAA AGTGCTTTTC CCAGTGAAGT 420
TTCTAACATT GCTAAAGAAC ATAAAATATA AAAACATGGC CATGCAGCAG GGGCTTTTTA 480
CCCTGCAGAA TGCCCACTAA ACCGTTTCTG TATGTTTAAT TTTTTTAACC AAGGAAGTAG 540
GGGATGCCCA AGATTTGGTC CCCAAACCAG AAAGACTGTG GGTTCCTTGC ATCAAGCCGG 600
GGCTTTTAGT CAACTCTCCC ATGGGGACTC TGTTGGCCCG CTCCACCTCG GGTGTTCCCC 660
CGCCCCTGCC TTTTCCTCTC TCACCTCCCC CATCCACCCC TCTCAGCCTT GCAGTCGACC 720
TGCCTCTCCT CTGGTTGCTC CGTTTGTAGG GAGGGTCTGC TTGAAGGGAG TTCCCATTCT 780
CTCTCACCCA GAGTCAAGGC TCTTGACTCT ATTGTACCTA AAAAGCTCCT GAGGAATTTG 840
ACAAGGCCCC ACCCTCAGAG ATATGGGGTG AAGCCCAGGA ATCTGTATTT TTAACAAGCA 900
TCCCAGGTGA TCCTGATACT TGCACACACC CCCACACACA CCCACGCCGA CTACCCACAC 960
ACTTCCATGG CCCAGAAGTC TGCAGGACCC ACAGCAGGTA TTCGGGACTA TTTGTTCAAT 1020
CCACACCTGA GTCGTTGCAC GATTATGCTC AAGTCCCTCG GAACACCTCG CCTGCCATCT 1080
GACAGCTTCC CATCCAGAAA CCACACAGTA CAGTAAAAAA CAGAAAAAAG AAAGCCGTTA 1140
GACCCCAGTG AATGTTATTT TTAATGAAAG TGGTGCATTT TGACTCACAA TGTTGAAACC 1200
AGATTATAAA TGAGTCATCA GTGAATCGAC CACAAAGAGC CTTTGCGGAG GTGATTTACA 1260
GGAGAGCTCT GATGTCTGCT GTCCCCTGCA CACGCTTCAC AGAGATGCTG TCAGACGCAG 1320
AGCTGGTCTG GGGCATCTGT TGCCGCGTCA GCTCAAAAGG ATGCTGTGTT GTCACCAATG 1380
GGATTCCCCA GCCCAGGCGG TGTTGCGGTC CCACCCACAC AAGGAAGGCG GCCATCACTG 1440
AATAATGCTT GTGGTTACAT CATCATTGCT GGTTTCCAGG TAGTGACTAG CAGATACTGG 1500
AGAGAGACAG GCCATCTGCT CTTCCTGTGC GCCTCAGCTC CTCCCTCATA CCCACATCCT 1560
CTCGCCTGGT CTTCTAGAAG CAGCCCCTAT GCAGACAGAC CAGCAGGACT GAAAGCTGGA 1620
CAGACTCGAG CCGGAGAGCC AGGTGGAACA ACCTGGCCAG AAAGAGTCTG GCCGCAAAGA 1680
GTCTGGCCAC AGCCCCACTT TCCTCATCTC TAAAATGTCC ACATGGCTGC CTGCCCTGCC 1740
CGGCTCAAGG GAATGTTGCA AGGCTCTCAT GGAAACCATG CTTGTGAGGG TTTTGAGGAC 1800
TATCATAGCC CGTCCCAAGG TCAGAGGACA GTAGAAAACA AAAAACTTGC TTTCAGAGGG 1860
TGCTTTCACC AGTCAGCAGC CTCTGCCCCG GGCAAAGCCA GACAACTAAA ACGGAATGAA 1920
TCCGCAGAGT AGGGTGGGGA TGAAATTCTC CACCTCCAAC CCAGAAAGGA AACGCCAATG 1980
CTCATGTTTC CCCTTAGAGA AACAGGCAAT GTTTGAACAG GAACAACGAC GCCAGAGGGT 2040
CAATCCACAC ACAGAACACT CCATCTCCAT GCCGATGGGG GACTGACTGT CCTGCTGCTG 2100
AACTGCACCC CTGGGGCTCT CCAGGACACT CCACTGGTGG CCACACTCAG GAAAATAAAG 2160
AAAAACCTTC AAAAGGACCC TTCTGGCCAT TCAGAGAATG CACAGGCCTG CTAGCTCCTG 2220
CTTGCCTGCT CAGAGCTGCC TCCACTGGGG CAGGAATCTG CAGCCAAGAA AATCCCTGAC 2280
AACCCCAGGG ACAGAAGGGT CAGTCTGGGG GACCATCGAC CAACCCAGCA ACCCAGATTA 2340
GACTGCTCCA CCAGGAACTC TGTGTCCAGA GAGCAGGATC TGCCACAAGC AAAACTAGGC 2400
CTCATTTACT ATTCCACAAT AGCAACTAGA AAGCATGTGA CCCAGAAAAC CTTCAAAGAA 2460
GGCCAGAAAT TCATTAAATC TGAAAAGAAG GGAAGAAGGG CGGGGGAGAG GAAAACACTG 2520
CTTAGCAAAG CCAACTGAAT CCCTCTTCCA TACATCACAG ATGCAGGACC AGTCTCAGCA 2580
TTCAAGAGGA AGAGAAAAAT GAAAACAAAA ACCAATCTGG AGTTGAATGT CAGCCTTCCC 2640
CTCACTGGTT CTGGGTCCTT TGGAAGGCCA TATTGTCCCC GGACCTCTCT TGCTTCAGTG 2700
GCCTTCCTGC CAGGATTGCC ATAAGGATTA AATGGACTCA TATATGTGTT GTACCTATAC 2760
AGTACCTGCA ACACAGTAAA TATCCAATAA ATGTTGGTTT CTTGCTACAA GAAATTGTAA 2820
AATATGGGCA CAAATTCCTC CTACTTTGTT AAGCACATCC CTTGGCAATG ACTTAGCTGC 2880
TACTCCCATC AAGAGTTGTG GTCTATGTCC CTACCCCTTG AATCTGGGCT AGCCTGGGAC 2940
TTGCCTCAAC CAGTAGAATT TAACAAAAGT TACAGTGTGT GACTTCCAAG GCTAGCCCTT 3000
GCCGCTTCCA CTTTTGCCCT CTTGGAATGT GGCCCAGAGA CAACCATCTA AGGAAGCTGA 3060
TCTAGGCCAC TGGAAGAGGG GTGGGCAGAT GGAGAAGTGA TGTCCCCCAA CCAGCTGCCA 3120
GTCACATGAG AGAGGCCATC TCAGATCTTC CGGCCCAGCT GAGCATTCAA CTAAATGCAG 3180
TCACATTAGT GAGCCCAAGC AAAACCGGCA GAACTGTCCA GACAACTCAT AAAATCAGGA 3240
AAACAATCAA TTCTTGTTTT TTTTGTTTGT GTTTTGAGAT 3280