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

TagContent
EnhancerAtlas ID
HS091-34380 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr3:56735650-56737300 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11130543chr356736942hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr3:56736708-56736727ATTCCAGCAGAGGGCAGCA+6.28
GATA2MA0036.3chr3:56736167-56736178ACAGATAAGAA-6.14
Gata1MA0035.3chr3:56736167-56736178ACAGATAAGAA-6.62
Nr2f6(var.2)MA0728.1chr3:56736397-56736412GAGGTCAGGAGTTCA+6.22
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr35673648356737094
chr35673712456737216
Number: 1             
IDChromosomeStartEnd
GH03I056702chr35673642956737028
Enhancer Sequence
CCACCATGCC AAGGTGTTTT AATTGTTTTT GGTGTTTTGT TTTGTTTTGT TGTTTTGTTT 60
TGTTTTTGAG ACTCTGTCTC TCAGGCTGGA GTGTAGTGGC AAGATCTAGG CTCACTGAAA 120
CCTCTGGCCC CTGGGCTTAA GCAACCCTCC CACCTCAGCC TCCCAGGTAG CTGGAACTAT 180
GCAGGTGAGT ACCACTGCAC CCAGCTAATT TTTGTATTTT CTGTAGAGAT GGGGTTTCAC 240
TCTGTGGCCC AGGCTGATCT TGAACTCCTG AGCTCAAGCA ATTCACCCAG CTTGGCCTCC 300
CAAAGTGCTA GAATTACAGG TGTTTTAAAA TAAGCCAAAT AAAGGATATA AACACTTCCA 360
ATTCATAATT CAGATGTAGA GGACCTTACA ATAGTTAACA ATTTTCAAGC TAAAAATCAC 420
ATCATCTATA AAACATTATA AGTGTTTTCC TTATTGAAAT GGTTTAGCGG AAGGCCGTAG 480
GGCTTGAAAT GGAGTGACGG AACACAAACA TGTAAGAACA GATAAGAAGA GTGGATGGTT 540
AGTTTAGGAA GGTTTTCCCT TTCCATTCCA AGACTAGATT CTGGCAATAT CTGGTATGTC 600
AAACTAAGAT ATGTAACATT TAAATACACA ATATTATTTT TATTGTGAAA ATAGTTTAAA 660
TATGTTTAGA ATATAAAATT TGGGCTGGGC ATGGTGGCTC ACACCTGTAA TCCCAGGACT 720
TGGGAGGCTG AGGCGGGCGG ATCACCTGAG GTCAGGAGTT CAAGACCAGC CTGGCCAACA 780
TGGTGAAACC TTGTCTCCAC TGAAAATACA AAAATATAGC CAGGCATCAT GTGCGTGCCT 840
GTAATCCCTT GAACCCGGGA GGCGGAGGTT GTAGTGAGCT GAGATCTTGC CACTGCACTC 900
CACACTGGGC AACAAAGTGA TATTCCATCT CAAAAAAAAA AAAATTGTGC CAGACGCTTG 960
CAGAACGCCT GAGACACCTC CATGAAATTC TAACAATGCA TACTAAATGC TTTATAATCC 1020
TTCTGTTGAA AACCAGACAT TCAAGAGCAT ACAGCTTAAT TCCAGCAGAG GGCAGCAAAA 1080
CTTCACTAAG CAGTTTTCAA AACCCTAGCA GCTTTTCTGT ATTACCTAAT AATATTTTTA 1140
AAATATTCCC CCAGAAGAGT TCTGTAGTTC CACAACTACA ATCTCATAGT ATTTGTGGAA 1200
TTACAGTATT ACCATACTTA TATTTAGGCA GGACAGAATT CTTCCCAGAG TTCAAAGACT 1260
GCGGAAGGCT CTTAGATGGA TAGGACCTGG GGCAATGCCA AGAGGGAATA AAGACGAGCC 1320
ACAATGTCTT ACTGGGGTCA TCTGCCTGGT GGTTTTCCAA CTCTTTTACA AAGAGTCATG 1380
ATTTAAGGTA CAATGGGATT CTTTTAAAAA ATATGTTGTC ACTGCAGGTA TGGTGGCCCA 1440
TGCCTGTAGT CCCAGGCACT GGGGAGGCTG AGGTGGGAGG ATCACCTAAG CCCAGGAGTT 1500
AAGAGTCCTG CCTGGGCAAC ATAGTGAGGC TGCATCTATA AAAGCACGCA TATATATGTA 1560
TATGTGTGTG TGTGTGTGTG TGTGCATATA TATGCACACA CACACACAAA ATATATATAC 1620
ACACACACAT ACTCACATAT TTTATAGTTG 1650