Tag | Content |
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EnhancerAtlas ID | HS175-17826 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr21:30095790-30097220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr21:30096737-30096748 | ATATTTACATA | - | 6.62 | Foxd3 | MA0041.1 | chr21:30096871-30096883 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr21:30096875-30096887 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr21:30096879-30096891 | GTTTGTTTGTTT | + | 6.32 | POU2F2 | MA0507.1 | chr21:30096669-30096682 | ATATGCAAATAAG | - | 6.57 | Pou2f3 | MA0627.1 | chr21:30096667-30096683 | TAATATGCAAATAAGG | + | 6.06 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTCTCTCTG TTACTTATTA CCCTGGGGAT CTTGGCATAT CACAGAGTTT CCAAGGGCTT 60 TATTTCTAAA GAGAAAAGAT GGAACAAAAG GAAGAAGTTT ACACAGAGAT TAAAAATCTA 120 AAACAGGGCT CAGATTCTTG CTCTTCAACT TCAAGTTTAA GACGTTGGCC ACATTACCTC 180 TTGGAGCTTG TTTCTTCATC AATAAGATGT TGATAATCAT CCCCGCCTCA TGGGACTGAT 240 GAAATGAAGG AGTGAGATCA TCTTTGTAAA GTTTTAGCAC AGTGTTTAGC CTGGCACGTA 300 CTACGAACCC AAAAATGATT TTTTAAAATT AGATGATAAT TCAGCTTCTT TCCAGCTCAG 360 ACATGCTATG AAGATACGCA GCCAGCACTG CCTTGCCATG GTGTGTCTTT TTTTCTGACT 420 CAAGCCTGTT CCTTATTAAA ATGCTGCAAC TTTGTGGTGA GAAAAGGAGT TATTCCGTAA 480 CTTTGACCAT CAGAAAGTGA ACCAACTGAC ACCAAGGCCT CAGCAATGAT TCTAAGTATT 540 AAGAGTTGCT TTCATCTTCA CAGATGGAAG AAGTGAGGAC AATACTTGGT CAAGGTCACA 600 CACGTTGAGG AACCACCCAA GAGAGATCAG AAACTCAATC CCTTCCTCAA GCCCTTGGAC 660 TCTGTTTGCT AATTACTTGT GAGAGTTATT AACGTGCTTT TTATTTTTCT TTAATTTTGG 720 TTTTCTTCAT TTATGGCTAT CAACATAATC CCTTGCTCAA AGCTCAAGGC TAAATACTAG 780 GTAAGGCTCA TATTCTCACT GGCAGAAACC TCTGTTTTAA ACACTTCTCT AAAAAATAGA 840 ACCTTGTTTA TAAGCTTTAT ACCATTGCTG TAAAATGTAA TATGCAAATA AGGCATTTTA 900 TAACTTTAGA GTTAAATAAT AAAGGCAGCA CTCCAAACCT CAACTAGATA TTTACATAAT 960 TGCATTACTA GCATTTGCAT GAGCTGTAAT GAAAGCTAAG GGGGAAAACC TGCTTATTTC 1020 CTATTAACTC CATAATAGAA CATGATTTTT ATTTGCTCTT ACAAATAAAA CTTAACTGCT 1080 TGTTTGTTTG TTTGTTTGTT TTTTAACCAG ACGCTACATT TGGGTTCCTT ATAGTTCCTG 1140 ATTATAATAA CAGAGCGCCA GCAAATTTCA TAAGAAGAAA AACCTGTTTG ATGAAAAATT 1200 AGTTATTCCA AAAGAATTCC CCTAAACATC TGACTTTAGT ATGCCTCTGC ATTTGCTTTC 1260 TGGCTTTTGA CAGATCAGCT TCTTCACTAC ATGTATCAGG TTTTTTGTTT TTGTTTTTGT 1320 TTTTGTTTTT TGAGACAGGG TCTCACTCTG TCACCCAGGC TGGAGTGCAA AGGCATGATC 1380 TCAGCCCACT GCAACCTCTA CCTCCTGGGT TCAAGTGATT CCCCTGCCTC 1430
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