Tag | Content |
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EnhancerAtlas ID | HS053-02696 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:157075960-157077200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr1:157076373-157076387 | CGATGACGTGGCAG | - | 7.58 | EWSR1-FLI1 | MA0149.1 | chr1:157076969-157076987 | GGAAGGGAGGGAGGTAGG | + | 7.47 | IRF1 | MA0050.2 | chr1:157076086-157076107 | TGTTGCTTTCTGTTTCCTTGT | + | 6.21 | PLAG1 | MA0163.1 | chr1:157076235-157076249 | CCCCCCTGCGCCCC | - | 6.09 | ZNF263 | MA0528.1 | chr1:157076211-157076232 | CACTCCCCTACTTCCTCCTCA | - | 6.01 | ZNF263 | MA0528.1 | chr1:157077071-157077092 | CCCTCTGCCCACCCCTGCTCC | - | 6.33 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 157076623 | 157076738 | chr1 | 157076072 | 157076782 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I157105 | chr1 | 157075492 | 157077336 |
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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
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