Tag | Content |
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EnhancerAtlas ID | HS098-14338 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:105776340-105777520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:105777300-105777319 | TACTTCCCCCTGGTGGACT | - | 6.3 | FOS | MA0476.1 | chr12:105776556-105776567 | TCTGACTCATT | + | 6.32 |
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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 |
GH12I105382 | chr12 | 105776296 | 105777580 |
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Enhancer Sequence | CTATAAGAGA GACAGGAAAT ACTGGCTTTC TGTTTGTGAT GAAATGCAAA TTCCTTATGT 60 ATTTTTCCAA AATGTTTAAA ATGAGGCTTT TGTAATCAGA AGTATATAAG CCCCCTTCCC 120 CCAAAGAAAA TGATTATTCT ACTGCCCGTC TTGACTGTAT TCTTACTTGG GGGCAGGGTG 180 GGTGGCGTGA ACAGGGAGAG CTAATCTCTC CTTCTTTCTG ACTCATTCCA CAGTCAATCC 240 TTTTTCTTAT TATTTTCCAA AGGCATGAGG ACCTTCCATG TTCCGAAACC ATTGTCCAGA 300 GTATTTCTTC TGGACTATTT TCCACTTCCT TCCATCTGAC CGGCCAGCTG TTCTGCATTT 360 GTAAAAGCTG GTTTCTGATG TCATCTCTAG GCAGGACCGC TCCCTCCCTC TCCTGCACTC 420 CTATACTTCG TGGCATATCC GCCCCAAGAT AACACTTGTC ACTCTGTTTT CCAAATTCAG 480 TTTCATTCAT TTGCTTCACA TGTGCACTGA GCCCACTGAC TTCTTTCCCT GTCTGTTGCC 540 AGCACTGGAG ACCAAGCCTG CACGCTTTGG CCCAGACCAT CTCATTCACC TTTTAACACA 600 GAATCAGGGT GAGTGGAGAG TGGGGGAGTG GTGTGGTGGG TCTTTGCCTC TCGCTGTTCA 660 GTGAACTTCA TGCCTGTCCT CCTGATCCCC AGCGCTAACA CAGGGTCAGG CTCGCGGGAG 720 TGAACAACCA CCATTTATCT CCGGCTTGTT GGGGGAAGCC CTTTCATTTA CTTGACAGTT 780 TACCTGTCAA TTTTACGTGC GTGGTCATTT TTAATCCTCT GCACTTTCAG GTAATAGGAA 840 AATAATTTGA ATCAAGTTCT TCCTTCACCA TTGGCGTAAA ATCGGTGATT AAACTTTTAA 900 TATTTAACGT CTTAAAAAAA ATTCCCCGGG CTAGCGTCAT GCCTAAGTAA TGCATGCATC 960 TACTTCCCCC TGGTGGACTC ATCTTCTAAT AGCAGCTTTG TTTTCCCCCC TTTATTATTG 1020 GCAGGAGTAA TCCATCTCTC ACTTTCCTTA ACACAGATAT TCATGGATTG CAGGATTCAG 1080 CAGTGTCTTC ATAATAGCAG GAAGTTTATG TTCTGGCTTT GCCACTTACT AGCTGTGTAA 1140 CTTGGGCAAT TTACTTAACT TCTCTGCGTC TCGGTTTCTT 1180
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