EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS062-04315 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr12:123385710-123388690 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs76465767chr12123386495hg19
rs10847980chr12123387922hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RUNX1MA0002.2chr12:123386226-123386237AAACCACAGAG-6.14
SCRT1MA0743.1chr12:123387570-123387585ATTCAACAGGTGTTG+6.02
SCRT2MA0744.1chr12:123387570-123387583ATTCAACAGGTGT+6.27
ZfxMA0146.2chr12:123386008-123386022CCCGCCTCGGCCTC+6.01
ZfxMA0146.2chr12:123386882-123386896GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_11355chr12:123370263-123387549CD20
SE_15159chr12:123385581-123386941CD4_Memory_Primary_7pool
SE_20678chr12:123382266-123386976CD56
SE_23035chr12:123382364-123387019CD8_primiary
SE_23125chr12:123387619-123388661Colon_Crypt_1
SE_23796chr12:123387734-123388477Colon_Crypt_2
SE_25026chr12:123387562-123388618Colon_Crypt_3
SE_28186chr12:123387496-123388807Fetal_Intestine
SE_29262chr12:123387470-123388856Fetal_Intestine_Large
SE_30119chr12:123385953-123386805Fetal_Muscle
SE_40937chr12:123385916-123386508Left_Ventricle
SE_43888chr12:123385114-123387000MM1S
SE_50159chr12:123387672-123388725Sigmoid_Colon
SE_52477chr12:123385818-123386540Small_Intestine
SE_52477chr12:123386628-123386944Small_Intestine
SE_52477chr12:123387587-123388622Small_Intestine
SE_53586chr12:123385804-123386506Spleen
SE_53586chr12:123387870-123388700Spleen
SE_61538chr12:123340041-123395084Toledo
SE_62830chr12:123354785-123387061Tonsil
SE_65302chr12:123388142-123388747Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12123387445123388309
chr12123387803123388391
chr12123386049123386659
Number: 2             
IDChromosomeStartEnd
GH12I122898chr12123382581123386981
GH12I122903chr12123387664123388509
Enhancer Sequence
ATTTTTACCT CTTGTGTTGA TCAACCCAGC CAGGGAGAAC AACTGCAAGA CCACTTAACT 60
TTTTTTTTTT TTTTTGAGAC GGAGTCTCAC TGTCGCCCAG GCTGGAGTGA GTGGCACAAT 120
CTTGGCTCAC TGCAGGCTCC GCCCCCTGGG GTTCACACCA TTCTCCTGCC TCAGCCTCCC 180
GAGTAGCTGG GACTACAGGC GCCCGCCACC TCGCTCGGCT AATTTTTTGT ATTTTAAGTA 240
GAGATGGGGT TTCACTGTGT TAGCCAGGAT GGTCTCGATC TCCTGACCTC GTGATCCGCC 300
CGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACCGCGCCT GGCAAGACCA 360
CTTAGCTTTT GCTTCCCTTA TGAATGATTT CTCTGGTCAC CCCTAGAGAG GACCCCAACT 420
GTTTTCAAGT CCCAGAACCT TGCTTTCCTC ATTAAAATAG CCTTCAGAAA GTGGCCCTGC 480
AGCATTTTTT GCCTGATTTG CCTTGACACC GCAGATAAAC CACAGAGGCA ACAGCCTGTT 540
CTCTGCTTAT ATGCATTGCG ATAAGCCTGA CAGTTTCAAG AAGATTAGGT TCATCCACTA 600
AGAAATTAAC TCAGCTCTAA CATTCACCTC GAACCCTGAC AATGTTGAAA AACCTTACGT 660
CTAAGTGGTT ATAACACTTG AGTTGGTTTA CACATAGGTA AAAGTACAAA GACAGGATTT 720
CCAGGCATTG GGTTTGCAAA TTCTCTAGAG AGAAACTAGA AACTGAAACC CTCTCAAGGT 780
GGTTTTTTGT TTTGTTTTGT TTTGTTTTTT TTTAGGAAAC CTTTATAGGT TTTTGTTTGC 840
TTGCTTCTTT AGTTACAAAA GTAATTTGCA CCTTGAATTT CTTAACTGAG TCATGGGCTT 900
ATATTATTAT CTATTCCTTT TGATAAATTT GAACTATTTA TAATAAAATA TACAAATTAA 960
CATCCAAATA CTTAAAAATA ACGTTTGTTT ACTGTAAAAA CTGTCTAAAC TGTGAGAAGT 1020
GTGTAAGCTG AAAAGTTAAC AACAAACCCT ATTGAACCCA TGTCCCAGAG GTAGCCACAG 1080
TGATCAGTTT TGTTTCGGTT CTAGAATTTT TAAAAAGATA AACATGTACG GGCTGGGCGT 1140
GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCGGGTGGA TCATGAGGTC 1200
AGGAGATCGA GAACAGCCTG GCTAACATGG TGAAATCCTG TCTCTACTAA AAATACAAAA 1260
ATTAGCCGGG CGTGGTGATG CATGCCTGTA ATTCCAGCAC TTGGGAGACT AGATGGGAGG 1320
ATCACCTGAG CCCAGGAAGT CGAGGCTGCA GTGAGCAGTG ATCGTGCCAC TGTACTCCAG 1380
CCTGGGCAAC AAAGGGAGAC CCTGTCTCGA AAAAAAAAAA ATTACCTGGG TATGGTGGCA 1440
CATGCCTGTA GTCCCAGCTA CTTAGGAGGC TGAGTCAGGA GGATTGCTTG AGCCCAGGAT 1500
TTGGAGGCTG CAGTGAGATA TGATCGTGCC ACTGCTCTCC AGCCTGGGTG ACAGAGCGAG 1560
ACCCTGTCTC AAAAATAATA ATAAAATGGC ATAAAATAAA ATTCAAATAG TAGATAAGGG 1620
GGTCAAACAA AAACCATTAA CAACTTGTGT TTCCTTCCAG AAGTTTTTTC AGTGCTTATT 1680
CAAGCAACTA TATTCATATC CACCCTCCTA CCCACTTACT TTTTTTTTTT AAAGCAAGAG 1740
AGATCACACT CTACTTATAT GGAACGTGTC ACTTTGCAAT CATATAGCTA AGGACAAATC 1800
AATATAACTC CTTAGCGACA TTAGCTGACC CATAGCTGGT TCCAAAAACT CTTGAAACCT 1860
ATTCAACAGG TGTTGCCTGA ATTTACCTTT CCCCTAGTAG TGCTGAAAAT AACGTTGGTG 1920
TTTTTTTTTT TTTTTCCTTT GAATTCCATG CAGGGTGTTT TCTTCTTTTT TTTTCAAGTG 1980
AAGATTCTTC TCAGCAGAAG GTGTTAATCC AGGCACTAAA TCTGGAACAT TCTAATCACT 2040
GTGAAATTTT GCATGTCTCG TCTTAGGCAG AAAATGTGTG AAGATACCAG TTTATTCTGC 2100
TCTTACCTTG CGGTCCTTCT CGAGGTGATT CTGCATATGC TAATGATCTT ATGTCAGCTC 2160
CCACCTCAGT CACCCCCACC TCTTCACCTC CTGGACCTGT TGCCCTCAAC GTCAGTGCTA 2220
CAGAAACCCA CCTAGTTTAC GCTCTTCTTT CAAGAGGGGG GTGCCTTATC TGATGCACTC 2280
GAAATCTACT CCCTCCTCCC AAGCCTTTCT ATTTATATAA CTGCATAATG TTTAACTGTA 2340
CAGGGAAGCT ATGAATCCTG TATTCATTTC CTATGCTGTG ACAAACAACC ACTAACTTAG 2400
TGGCTTAAGC AACACTCATT TCTTCTCTTA CAGTTCTGCA GGTCAGAAGT CCAAAATCAC 2460
GAAGTCCTAA AGTCAAGATG TTGGCAGCCC TGGTTCTTTC TGGAAACTCA GAGGGGAGAA 2520
TCAGCTCCCT TGCTTTTCTC CCAGCTTCTA GGGGCCTCGG TCAATCTCTG CCTGTTTTCA 2580
GATTGCCTCC TCTGACCCTG ACGCTCCTGC CTCCCTCTTA GGAAGCCTTT TGTGATGACA 2640
TTGGACTCAC CTGGATAGCC CAGGCGCCAC TCCCCACCGC AAGGCCCTTC GCTTAATCAG 2700
ACCTGCAAAG ACCTTGTACC ACACAAAACA ACGCTGGCAG GGCATGAGGA TGTGGGTGTA 2760
ATTGGGGAAT TATTATTTAG TCTTCCACGC CATCATCCTT TACAAATAAA TAAATTAGGA 2820
CAAAGAAACT AAGTTCTCCT TGGCCACCAA CTGTTCATCC TTTCTCCCCA TGGGCGACCA 2880
CTGTTAACAC TCCTTGGTGT GAATTTTTCC AGACCATTTT TATTCTTTAA CATATATACA 2940
TATGAATGCA CAACAGATTT ATTTAGTGTT GTTTTGGGTA 2980