Tag | Content |
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EnhancerAtlas ID | HS053-10855 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr13:27768990-27769990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr13:27769629-27769650 | AGAGGAGGAGGGAGTAGGAGC | + | 6.11 | ZNF263 | MA0528.1 | chr13:27769651-27769672 | GGAGAAGAAGGAGGAAGATGA | + | 6.12 | ZNF263 | MA0528.1 | chr13:27769636-27769657 | GAGGGAGTAGGAGCAGGAGAA | + | 6.26 | ZNF263 | MA0528.1 | chr13:27769645-27769666 | GGAGCAGGAGAAGAAGGAGGA | + | 8.32 |
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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 |
GH13I027194 | chr13 | 27768224 | 27770659 |
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Enhancer Sequence | TTGAGCAGTA AAAGCAAGAT TCTGTCTCCA AAATAAAGAA ATAAATAAAA ATATTTATCA 60 GCTATTACAT CCAACATTTC CATTAACATC CCATTGGCCA AAATTTGGTC TCATAGTCTT 120 GTCTAGCAAT CAGGAGGCTA GGAAATAGTC TTTATTCTGG GTGGGCGTGT GCCTAGCTAA 180 TAACTGGGGG TTCTAGCACA AACAAAGGAG AGAATGGATA TTAGAGAGGA AAGGAGCATT 240 CCATTCCCCA GCTGGGTGGA TAACAAACTG CCTCTGAGCA AGAAACATAA TGAAAATATT 300 CAAACACAGG GAAGGCTGCC CCAAGATTGA CTTATTTGTT TATTTATTTG TTAGGGTATA 360 ATTGTCAATG GTTTACTTAT TGTGTCTTAT AGAATCATAA GCTAGATTAT GTCCTCAGCC 420 CTCCTGGAAA TGCTTGGCAG AGTGTGCGTC CCATTCAACC TCCACAGCGT AAAGGAAAGG 480 GAAGGCACTT GGGGAGATTT CAAAGAAAAG CCACCAGGAT GACTAATAGC TCAAAACAAT 540 AAGACCTAGG ACGCACTGTT AAGGAATGAG TCAGCCAGGG AAAGAGATGG CTAGAGGGTG 600 ACTAAATAAT GATCCCTTGC TATACAAAGG TCTCTGCACA GAGGAGGAGG GAGTAGGAGC 660 AGGAGAAGAA GGAGGAAGAT GACCAGGAGT ATGGTCATCT CCACTAGGGG TTGAACGGAA 720 GGAAACGGGA GCAGGAGTGA CTTAAAGATA CCTGAAAGGA CAAATGTGCT GAAGGGGATG 780 CTTGTCAAAA TACAGGAGAT GGTATAAACA TATAGCACGT GGGGATTATA CATTGGCATC 840 TCTGACCACC GTGGTATTTG AATGTGCTCT TCACTAAAGC AAAGCTTGAG AGTTTGCGGG 900 GAGGGAGGGG CATTCACAGG TGGAGGGAGG GTGAACGACC AGAACTCCTA TGATTTCCTT 960 CTCTGTGCCT CAGTTTCCCT CATGGAATAA CCATGTGTTG 1000
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