| Tag | Content |
|---|
EnhancerAtlas ID | HS139-19494 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr15:83917040-83918260 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr15:83917326-83917345 | ATTCCAGCAGAGGGCACTA | + | 6.6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCCGGAGGG GCTCTGGATT CAGCTTCTTC TCCCGGAAGG CAAATGCCAT CTCGGGAGTT 60
GCGGGGGAAG CCCGTGGGAA ACCTACTCCA ATCCAATGTT CTAGGCTGAG GCACTCAATT 120
CCTGGAAGCA GGATTAAGAC CATTCAGAAA ATATGTCCTC TTTTCAGCTA GCCTTGTAAC 180
TGGAAGAGGT ACATGGGGTC ACCAGGGGAC TTTCCAAACA TAATACATCT CGGAGGTCTG 240
AAAGGACTCA GAAGTAGCGC ACAATGCCTA TTGCAATAAC CAAGTAATTC CAGCAGAGGG 300
CACTATTTCC TAACAATCTG AAATGCTAAC CAGCATCACA GATTGGAAAG CTAGGAAGCT 360
CCTTTAAAAA AACAATTTTT TTTTTCAGTA GTCTTAGCTC TCTGCAAAGA ACATAAGTAT 420
AGCAATTCAG ACTAATTAAA ATTCCCAATC ACACAGATTT CTAGGGTGTA GTTTTAAAAG 480
AATCAGGTGA CCAATAGGCA TTCTGTTCTT TAAACAGTTT GCCTGTGGCT GCTTTTAAAG 540
TTTCTTGACT AATCTGGCTT TAATGATCAG CCAGAGCATG TCTTGCAGAA GAAAGAGCAA 600
AAGACGTTGA AGCACACTGA GCCAACCACA CATTTCAATA AATATGTAGA TTTTGAGACA 660
CTGTGAACCA ACATGCACAC ATTTCAATAA GTAGATAGAA GCATAGGGAC AGGGAACAAC 720
CCACACATTT CAATAGATAA ACGTGGAGGC ATTGTGAACC GACAAATAAA GAAAAAAAAA 780
GAGTTGTGGG TGAGAAGGGG GGTGACAGGC TGGGCTACCT GCTCAGGAAT GCACAGCTGG 840
TGTCCAGAGA CTCAGTCAGA TGCTTCTCTT CTAGCCCCAC GATTGCCAGG GAGCTAAGAA 900
CAGGCTCTCA TTTCCCCAGA TGAGGAAATC CTGGTCCAAA GGGGTTTTCC CTCAGGGGTC 960
TCAAGCTCCT CTGTAGATGC CCCAGCATCT GAGGAGGTGG GAGGAGAGGC TGAGAGAGGC 1020
TGCCCAAGTC AGGGACTGAG TCTTTTCTTC CCATGAACAG AATGAGTAGC AGGACTTTTC 1080
CCTTTTAAGA AGAGTCTAGA CCAGTGATTC TCAACTGGGG GCTATTTTGT CACCCACTCC 1140
CATCAGGGAA TATTTGACAA TGCGTGGAGA TATTTTTGGT TGTCATAATT TTGGGGGTGC 1200
TATGGCATTT AGTGGGTAGA 1220
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