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

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EnhancerAtlas ID
HS053-02696 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr1:157075960-157077200 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB3MA0638.1chr1:157076373-157076387CGATGACGTGGCAG-7.58
EWSR1-FLI1MA0149.1chr1:157076969-157076987GGAAGGGAGGGAGGTAGG+7.47
IRF1MA0050.2chr1:157076086-157076107TGTTGCTTTCTGTTTCCTTGT+6.21
PLAG1MA0163.1chr1:157076235-157076249CCCCCCTGCGCCCC-6.09
ZNF263MA0528.1chr1:157076211-157076232CACTCCCCTACTTCCTCCTCA-6.01
ZNF263MA0528.1chr1:157077071-157077092CCCTCTGCCCACCCCTGCTCC-6.33
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1157076623157076738
chr1157076072157076782
Number: 1             
IDChromosomeStartEnd
GH01I157105chr1157075492157077336
Enhancer Sequence
TCTTTGTTGC CCTACCTATC CTGCCCCTTG GAATGCCCAT TTCCCTCCTC TGGAGTGTTG 60
CCTGTCTCAA CACTTCTTTC CCAGCCTGGT GCTCTCTGTT TTGCTGTCTC TGTCACTGTC 120
TCCTGTTGTT GCTTTCTGTT TCCTTGTCTG TCTTTCCTCT CTTGCCCCCC ATCTCTCATC 180
CATGCTTTGG AGAAGGAAAC TGACCACAGG CCTCCCAGCT TCCCTGCCCT GCCCTTATAG 240
CACCACCACC CCACTCCCCT ACTTCCTCCT CAGATCCCCC CTGCGCCCCT CGACCTTCCC 300
CTAGTGGCAA CCTCATTCCC ATCAGCTGTG CCTGGGGGAG CCCCCTGCCT GGACACCCCC 360
TGATCCTTCC CTTTGTCCCC CCAACACAGA GACAAGAAAT CCCCTCCAGC AGGCGATGAC 420
GTGGCAGAGG AGCAGGTCAG AGGCAGAGGA AGTGAAAGCT CCTAGCAAAC AGCTGAGCTG 480
GATGAGCTGG CAGGGCCAGC ATGGGGCTGA GTAACTGGGA CCAGGACAGC AGCGTGAGAA 540
GCAGGCATCT GAGGCCATTC TCCCCAGCTG GGGGCCTCTG ATACCTTCTG ACTCAATCCC 600
CAACCCTCAA CCCTCATGTC CACTTCCAGC CTCAACCCCA ACCCCAATCT TAACAAGAAC 660
CTTCAACTTC CACTAAGCCC AAAGCCTCAT TGAAGGCTGC ATCCATGCAC CCTGGTCCCT 720
GTGCCCACTG GAGCCCCACT GCCCTTGGGC AGGACCAGAA AGGGGCTCGG AGGTGGCGAG 780
ACAGCAGCAC CACTCTCCCC AGCCCTTCTC CTCTTGTCTC CACTGGGAAG GAGTTGGTGA 840
GACGAGCAGG ACTTCTCTCT GCCACGGGAG CATCATCTCT GTGTCTCTCC AGCCTCACAA 900
GCCTGGATCT GCCCTCACCA TCACAGGGGC TCTCGTGATA AGCAGGAGAC TTCACGTTCT 960
CAGACTTTAG GCTTCTTCTA GTTCCTTGAA AAGGATCCCA AGAGTCTGAG GAAGGGAGGG 1020
AGGTAGGAGT GGGGCAGAAT CCTCTCATCC CATCAGAGGT TTCAATTCAG AACACCCCAG 1080
CCCGGATCAG GTGGGAGCAC AATCCTGGTG GCCCTCTGCC CACCCCTGCT CCTTCCCGTC 1140
CTCATGCTAT GAGGTCCACA CCCTCACCTG CCTCCCTCTG CCCAGTAGTA GCCACCAGCT 1200
GATTGTCAAT CCTCACCCAC TGATCTTCAA CCTCAGCCAC 1240