Tag | Content |
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EnhancerAtlas ID | HS001-08424 | Organism | Homo sapiens | Tissue/cell | 786-O | Coordinate | chr8:121012050-121013760 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr8:121012599-121012610 | GTCTTTGTTTT | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGAATTCA GTGAAGGAGG CCATAGAGGG GAAACACAGG GAGAGAGTTC TTCTGCCATG 60 ATTGTTGTGG TGGTTACAGA AATCTCTACG TGTGATAAAA CCGCACTGAA CTATATGTGC 120 TCCTGCACAC ACATGCACAC TCACACACAC AAATCAGTGC ATGTAAAAGC TGGTGACATC 180 TGAATAAGGG CCGTAGACTG TACCGATGTC AACATTCTGG TTTGATATTA TACTATAGTT 240 ATTTATGTAA GGGGTTACCA TTGGGAAAAT CTGGGTGAAG GGTACCCAGG AACTCTCTGT 300 ACTCTTTGCC GATTTTTTTT AACAGCTTTA TGAAGATATA GTTCACATAC CAAGCAATTC 360 ATTAAAGTGT ACAATTGAGT GGTTCTTAGC ATATTTACAG AGTTTTGTAA TCATCACAAC 420 AGGCAATTTT AGAACATTTT CATCACCTCA AAAAGAAATT GTGTGCTGTA GCTAATACCC 480 CTCCCAAACC AACCCCAAGG CCCCCCTCCA GCCCCTGGCA ACCACCAGTA TACTTCTGTC 540 TCTAGAAGTG TCTTTGTTTT GGACATTCCA TATGAATGGA ATCATACAGT GTGTGGTCTC 600 TGCATTTTCT TTGCAACTCT CTGTAAGTCT ATAATTATTT CAAAATAAGA AGTTATTTTG 660 GTTTTTTCTG AGACAGAGTC TTGCCCTGTT GCCCAGGCTG GAGTGCAGTG GTGCAATCTC 720 AGCTAACTGC AATGTCTGCC TCCCGGGTTC AAGTGATTCT TATGCCTCAG CCTCCCAAAT 780 AGCTGGGATT ACAGGTGTAT GCCACCACAC CTGGCGAATT ATTGTATTTT TAGTAGAGAC 840 GAGGATTCAC CATGTTGGCC AGGCTGGTGT CAAACTCCTG ACCTCAAGTG ATCCATCCAT 900 CCTGGCTTCC CAAAGTGCTG GGATTACAAG CTTGAGCCAC CGCACCTGGC CTCAAAATAA 960 AAAGTTTTTA AAAATGAATT GAGGGGCTGG GTGTGGTGGC TCACACCTGT AATCCCAGCA 1020 CTTTGGGAGG CTGAGGAGAG TGGATCAGTT GAGGTCAGGA GTTCGAGACC AGCCTGGCCA 1080 ACATGGTGCA ACCCCGTCTC TACGAAAATA CAAAAATTAG CCAGGTGTGG TGGTGGGCAC 1140 CTGTAATCCC AGCTACTCGG GAGGCTGAGA CAGGAGAATC GCTTGAACCT GGGAGGCGGA 1200 GGTTGCAGTG AGCCGAGATC ATGCCATTGC ACTCCAGCCT GGGTGACAGA GCGAGACACC 1260 ATCTCAAAAA AAAAGAAAAA GGATCGAGTG TGGCTATGAG ACAAGCTCTC TGCTGGGCAA 1320 TGGGGACACA TGAGTAAGTG AAGCCATGAT CACTGCCCCA ACAAGCTTAG AGTTTAGAGG 1380 GAAAGAGAAG GGGCAGACAG TGAGGGTGCA GTGTTATCAG TGCTTTGGTG GAAGCAGCAC 1440 AGGAGCCAGG AGAACACTAG GAAGAATAGA ACTCAGATTG AAAGCAAGGT CAGGCAAAGT 1500 TCCCCAGAGG AATTGGTTAG CAAATTTTTA AAGTGCATGT CACGTGGAAA GAACTTGGAA 1560 CCATGGGCGG ATGGGCGGCA GCTCATGTGG CATCTGTGGA AGAGAAGTCT TTCTTGAGAC 1620 TTTTGCCGCT GTTGCCTGCA GTCCTTTGGC TGTAGCGCTC AGTGGCCAGG ATGCCAGATA 1680 GTCCTCATTG GTTGTTTTTT TTTTTCTCCC 1710
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