Tag | Content |
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EnhancerAtlas ID | HS053-00683 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:24698690-24700190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:24699344-24699364 | GGTTGGGGTGTGGTCTGTGG | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26747 | chr1:24698158-24700792 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I024371 | chr1 | 24698159 | 24700792 |
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Enhancer Sequence | CAAAAACAAA AAAATCCAGC TGTTGGACAC TGGGCCTGTC ACCTGCTTTT CTATCTCCTC 60 TGCCTGTGAA GTGGGGATAA AAGAAGAAGA AGAGCTCACA CTTTCTGAGC CCATGATTAT 120 GTGGTGAGTA CCTGCTCCAT GGGGCTTTGG AGCATTCAGT GAGATAATGA ATGTAAGGCC 180 CCTGGCACCC ACGGGGAGCT TAACAGATGC TAGTACCCAC ACTTCCCCTC CTGTTCTGTG 240 TTATAAGGGG CTGGGGGCTT CTCAGGATCC CCCCACCCCG GGAGGGAGCA GGAGCAGGGG 300 CAGACTGTGG AGGTGCCCAC ATCCCAGGGC TCACTGGCAG GGACTCTGGC CAACCCCAGG 360 GATGCTGGCT TTGTTCTTCT GTATAAATAG ACAAGGTGGG GTTTTGCCCA TGGATGATGC 420 AAGGCAGGAG AGCATGAACT GGGGCTGAGC CTCCTAATTA GCGCTGGTTT TGTTATTCAG 480 CTTCAGATTG ATCTTTTCAA CTTTAATCTG GATTTGCTGA AATCTCACAT GCACTACAAT 540 TTTATCCACA CCCCTCTGCA AGAGGCATGA TTGCAGAAGC AAACCTTCCC TGCTCCTCCT 600 CCTGCTTCTG GGGCCCAAGG TTCCTGGGGC AGCTCTGGTG CCCAGGGCTT CTGGGGTTGG 660 GGTGTGGTCT GTGGGACCTA TTTGGGATAA TCTAATATAA TAAGTGCTCC AGCACTGGAG 720 GTCAGAGAGC ACAGGAGAGG TGCAACACCC TTCCCCAAGG CCGGCAGGGG AAACACTTGC 780 AGGAAAGCTC TTGTGTATTC CTGAATCTTG GAGGTTCCAG AAGGGACAAT GGAATGATGG 840 AGGACGTGGG CTCGTTAGTG AGACCCCTCT GGGCTTGTGT CTGCCATTTA CTGGCTGTGT 900 GACACTGGGC AAGTCATTTC AACTCTCTGA GCCTCCACTT CCTCATCTGA AAAGTAGGGC 960 TAAGTGGATG AACCTATGAC GGCAGACCTG CAAGACTGCA TGGAAACCAC TCACCGTGGA 1020 GTGGGTGCTC CGGAAACAGA GCTGCCTCCT CTGTTTTATG ACTGGATGAT GAAGTCACCT 1080 CTAGCATAGG AGAAAATGAA CGTGGCAGCT CAGTGTTGAA GGAACAGGAT GTATGGTCAT 1140 GCCCTGTATC TCCTGCCCCT CCCCAGTGGC CCCTAATGGC AGCTGGGGTA TACGAATGTG 1200 CACATTTCTG AGGTGAGAAG CCACTTCTCC ACTTGGCTGC CCAGAGCAGG TATGCCAGAT 1260 CATAAAAGGG GAGGCCAGGA AGCTGCTTTG GAGGCCCATT TCCAGAGCCA GCCATTGTCC 1320 TCCTGGTGGG GATTGCTGGC TGTCTTCTCA CCTCTCCTCT TTGTTCAGTA CCTGCCTGCT 1380 ACTCCTCCCC ACCCAAAGAC TAAATCCTTC CAAAGACTCC CTGTGAAGAA GTAGGTGCCC 1440 TGCAAATCAA ATCTGGGACA CTTAACCCTT AGGTCAAGGC CAGTGCAAAG CAGCTGCTTA 1500
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