Tag | Content |
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EnhancerAtlas ID | HS037-39784 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr9:23768850-23770220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:23769202-23769214 | AAACAAACAAAC | - | 6.32 | RUNX1 | MA0002.2 | chr9:23769431-23769442 | GTTTGTGGTTT | + | 6.02 |
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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 |
GH09I023767 | chr9 | 23767819 | 23771285 |
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Enhancer Sequence | TAGAAGCACA TCATGATTAA GTCGTGGATC ACCAGTGATC TTCATACTAA CTAGAAAAGT 60 TTAGGCAAAC AGAAACGATA ACATCTCTTA AAAGAATCAT GGCTAGAGGC AAAGACAAGC 120 TTATCTCTCA GGCTGGAAAG GTCCAGCCTA AACAGAGTGA ACTTGGTCTC TACACTTATT 180 TGCAACTAGA AGCTTTGAAT ACCCTGAGTA TTCAAACACA GCACACCAGG ACAGAATCAG 240 CCCAGTACAA AGGCCTTCCT TCTGACCACA TCAAACCTCT CCCTAAATGC CAAGTTACAG 300 ATGAACAGAA GACATTTGTC TCTAAAGTTT TAGAGCCAAA CATACAAAAC ACAAACAAAC 360 AAACAAAAAA CAAAACCAGG CATCACAACC TTTACCACAC CATCCTTTGG GGAACTTGCA 420 GCAGGGACAA AAGCACTCCA AAATTGGTGA AATAAGTCAT ATGAGCTTAT AGATGACAGC 480 TGGGTAGGCA GTCAAAGGGA TCATCTGCCC GACACACACC ATTCCTATAG CAAATGCTTT 540 ATCTTTCCCA TTCAAATCAC TAAGTGGTAT TTTCAGGATA TGTTTGTGGT TTCACTTAAT 600 TAAGCAAGAG AATAGTCAAC CAAGTGCTAA AATCACAAGG CTAACAATGT CAGTTACAGG 660 AACAAGCCAT TAGTTTGTTT TCTTTAACTC TCTTTGCTTT GTGATTCCTA AAATAAAGGT 720 TTGTAGCTTT AAATGTCAAA GGATTTATTC AATCTAGAAT CCTTGTCAAT TCTCCAGCCC 780 ACCCACATAC CATGTTAGCT GTCTCACTAG CTCTACGAAT TCCTCAAACC CACATTTTCA 840 GCCTTGGGGC TAACAACGGC CCAAGAACTT GCAGAGACAA TGCACTGAAC AGCTGCACGC 900 GTCATAAGGA GAATGTTCTT TGGCAGCAAA CACTAACGTT TTTCTGTCTC TTGGCCCTTT 960 ATGACTTCTA CGGACAAAGT ACACAGTCTC CTTCATGCCA GTCTTTCTGA GGTTTTGTAG 1020 TTTCAGAGCT GGCAGGTTCA AAAGCTTTGA GGTTAGAGAG GTAAGATAAT GAGTTTAGGG 1080 TCCCAAGTCC TTCTCTTCAG TCTAAGTCCA TTACAGGTAT CCAGTTTGAG CAATGGGAAA 1140 GTAAAGATCT GGCGAAAAAG ATCTGCTTAA GTTTCATGTT TTGTTCATTC ATCCATTCAA 1200 CGAACATCTC CATGCAGCTC CCACGAATTC AGGAGAGTCC TGAGGTACAG CAATGAAGAA 1260 GCATCTTGGA GTGCTGATTT GCTGTGGATG GTGTGTGCAG AACATATACA AGTATGAACA 1320 CATAGAAGAA AACAGTACAT CAGCAATAAG TAAGAGTGCT GTGGAATACA 1370
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