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

TagContent
EnhancerAtlas ID
HS091-00739 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr1:21920250-21922700 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs55722102chr121922132hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr1:21922203-21922222TGGCGCCGCCTTGTGGCCA-6.59
MAXMA0058.3chr1:21920920-21920930ACCACGTGCT+6.02
Nr5a2MA0505.1chr1:21921838-21921853GAGTTCAAGGCCACA+6.65
ZNF263MA0528.1chr1:21921153-21921174GGAGGTGGGGCAGGAGGAGAG+6.71
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_33659chr1:21911996-21920758H2171
SE_65280chr1:21921409-21922251Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12192178621922000
Number: 1             
IDChromosomeStartEnd
GH01I021594chr12192141021922251
Enhancer Sequence
GCTGCTGTTT CCACTACCAG AGTAATTTCT AAGCAGAGTC CAGCGCTTCC CGGAGCCTGG 60
TACCCCCCGC CCAAGTTCTA ATTCCAGCCT CGAGTCAGAG TGTCCCGGCT CGCCCTCCCA 120
CCTCACAGCC CAGGGTGAGC ACAGAGCTGG CGCGGGCACA AGAGAAATAG CACCGGACAC 180
TTTGATCCCA GAGGCCCGAT CCGTTGCCAG CCTCCCCTGA CCCCACCTCG GAGCTTGGAG 240
GGATGCGGTA GGGTGAAACC CAGCCCCAAG GCCTTCCTTC CCGCAGACGG CCTGGCACCA 300
GCTGGACAGG GATGGGGCAA AGGCAGGTTC TGCCCACCAA GCTGCCCACC TGCTCTGCCA 360
CAGCAGCCCC TGCTGCTCTG TCTCAGCTGT GGGATAGAGT GGAGTGGGGG TGCATTGCTA 420
AGTACAGGGA GACAAGCCGG AGACCTCCCC CAGCTCTGTT ATGGCAGCAT CGTCACCCCA 480
GGTAAACCTG GCAAGCTGAG GCCCAGGGAA GCACCTGACG CCGTCCATTC CCAAAGCCTC 540
ACATCTAGGC ACCTGTGCTG GGCCCAGTGG CAGGTGGGCG TCCTCCACGC ACTGAGCGGA 600
CCCCACGTGT TCTGAATTAC GGACGTCATT GATCCCTTCC TGCGGTATGC ACACTCTCTT 660
CTTTGAGCCC ACCACGTGCT GGGGCTGCAC CCAGAACTTT ATGAGGTGTC ACCTCATTTA 720
ATCCTCATGC CAGGGTGCCA GCGAGGGCAG GGCTGTTAGC ACCCCCACTG CACAGATGAG 780
GAAACTGAGG CCCAGGGAGC CAAAATCGTG TCTGCATGGT CATAGCGCGA GGAGGCGAAG 840
CAGCTCAGAG CTGATTCTGA AGAAGCTCTT AACCGTGGTG CTGAACTGTG ATGCCGGCCC 900
TGTGGAGGTG GGGCAGGAGG AGAGAGGGCA GAGGACTGCG GCGGAGGGAT AGGGAGCAGG 960
GGTGCGGCTG ATGGGTGGGC AGTTCACAGG GGACTCACTG GGCCCAGAGC AGCCTAGAGC 1020
CAAACCGAGT TGGGTGGGGC TGGGGTTTGG GTGTGAGTCA CCACCCATGG GTGGCCTGAG 1080
GCATCAGAGG GTCACAGAAG GGCCCTGTCG GGAAAAGTGT GGCACTCCCT GGACAAACCC 1140
CTGGGGTTCC TTCAGCATCA TCCTGGGAAG GGGGCAGGGC CAGCAGGGGA TAGGGGGCAC 1200
TGCCAAGCTG TCAGGGAGGC CAAGGCACGG CTCATCCCTT CGGGGCCCAA TTTGGTGCCT 1260
ACTCCCAAAT GTCCCCAAAG CCACCCCGCA GACCTGCTCT CCTCCGTGGT CCTGCCCCAG 1320
AGGGAGAGTC CCCTCATTCA CCCAACACCC AGCCTGTACC CCCGGGAGCC ACCCGATTCC 1380
CCCCTTAGCC CCACAGCCCA TCAGGCGCTT GGTCCCCCTG CTCAGGCCCA CCTGGTGTCC 1440
TTCTCAGCGT CCTCCTGGCC ACCCTCTTAC CCCAGCAACA ACCTCGTTGG TCCCCTCCTC 1500
CCTCCACTGG TGCAGCCTCC ACCAGCAACT ACCGCTCCTG CCTGGGGCTC CCCCTGCCCT 1560
TGGCGCAGAG CCCTGGCCTC TCCGTCGGGA GTTCAAGGCC ACATTGCCTC TGGCCTCATC 1620
CCTGCCCATC TCCCTGTCCC CTCCATTGTC ACCTTCCCAC CATTCAGAGC TGGCTGCCAC 1680
CTTCCTGGTT CCAGGGGTGC TCTGCCTCCC CGCCCTTTAC TCGAGGCCCC CTCCTGCAGC 1740
GTCCCTCCTC CCTAGGCCTT CTCAGGAACG GGGAGCAACT CCAGGAACTT TCCCTGACGC 1800
CTCTCTCCCC AGGCCCTGCT TGTGCACACC TCTCCTGTCC CCGGCTGCCC CTCATCACCC 1860
TTCGTCCTAC TGTCCCAGCT GTGAGATCCT GGTAGAGGGA CTTGGACTCA TCCCCGTCTC 1920
CTGGGTCCCC ATCGGGTCCC GTAAGTGGTC CCTTGGCGCC GCCTTGTGGC CATATCAGGG 1980
GATTCACTGA ATATGAGAAC AGGGAGAAGG AAGTAATTAA TTGAGCACCT AATGTGTGCC 2040
AGACACTGTG CTGTATGTTT GATACGCACC AGCTCATTGA ATCCTCACAA CAAACCCTTG 2100
GGAGAAACAC TACCACTCCT ATTTTACAAA AGGAAACACT GAGGCTCACG GAAGCTAGTA 2160
AGTTTCTCAA CGCCACCCAC CCAGCTAACA AGAGACGGTC CCAGGACTCA AACCTAGGTC 2220
TGCCTGACAG CACAGCCATG TTCTTCCTGC AGTGGGGAAG GGGCCCAGGA TGCAGGGAAG 2280
GACAGCACCC CGGGGAGGAA ACCACGGGCG GTGCTCACAG AGCTGGTGGC TTGGCTTTGG 2340
AGGTGTCCCC AGGCCCAGCA GCTCTGATGG GGACAGGCTT GCTCCCTGCC ACCTTGACAT 2400
CCCTGGACAT CTGTCTGGGG TCAATCTGGC CACGGTTCAC ACAAAGCCAG 2450