Tag | Content |
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EnhancerAtlas ID | HS139-15941 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr13:114930900-114932780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr13:114931310-114931331 | GGGGGAAGGAGGAGGAGGAGA | + | 6.43 | ZNF263 | MA0528.1 | chr13:114931323-114931344 | GGAGGAGAAGTGGGAGGAGGT | + | 7.13 | ZNF263 | MA0528.1 | chr13:114931314-114931335 | GAAGGAGGAGGAGGAGAAGTG | + | 7.64 | ZNF263 | MA0528.1 | chr13:114931311-114931332 | GGGGAAGGAGGAGGAGGAGAA | + | 7.74 | ZNF263 | MA0528.1 | chr13:114931320-114931341 | GGAGGAGGAGAAGTGGGAGGA | + | 7.87 | ZNF263 | MA0528.1 | chr13:114931317-114931338 | GGAGGAGGAGGAGAAGTGGGA | + | 8.25 |
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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 |
GH13I114166 | chr13 | 114931861 | 114932010 |
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Enhancer Sequence | TGAACTCTCA CCCATTAGAT TGACAGAGTG GTTCTCGACT GGGGTTGATT TTTGCTGCCA 60 TCTCTCCCCA GGGGACAGCA ACGCCTGTAA ACTCTTTGAG CTGTCACACT GGATGTGAGG 120 CACACCTACA GCCATAGAAT CCTAGAAGCC AGGGGTGCCA CCCAGATCCC ACAGCGCAAA 180 GGACATCTCC CCACAGCACA GAATTGTTTG ACCCAAAATA TCGCTTTTCA TCAGTGGCCT 240 TCTAAACTCT GCCTCTTAGG TGATAGGCTG CTCCCACCTA GGACTGCGTG TTAAAATGTG 300 AAAACGGGCG GAAGCTTGGC AGCATGCACA GCTTTAATCA GGGATTCCGT CTGGAATACC 360 TGCTGGGAGT CACTCTCTCC AGGTTAGTGG CCATCGTGAT AAGCGATTCT GGGGGAAGGA 420 GGAGGAGGAG AAGTGGGAGG AGGTCTTGGT GCAGCAGGAG GCATTTAAGA TGGGATGGAC 480 TGAGGAGCCG CAGTCGCTGG ATTGGACCCA AGCCACCAAG CTGGACCACA AATGAAGCCC 540 TGGATCCACA CCTCCTCCTG GTCACAGTGA CAGTTCCCAC CTAGGACATC TGACCTTCTA 600 AAGGCCAAGG CAGTTCTTTA CTAAGCAGAC GAATACTACT TTCTTCTCAA TTTCATTTTC 660 CTTCTCAGTT GGAGGAGAGG GTGCAGTTTG TATTTCATTG AATTTTCTCC TTTTCTTGAA 720 GGGAAGGATA TGTTGCCAAA AATACTCATG AACTGCTTCC TTGTTTTTGT GATGGAGAAA 780 ATGATTATTT ATTTTACAAT TGCATCTGCA TTAAGATGGC AACAAGGGGC CGTGGGCTGA 840 GGGGTTAGGG TCCTGTCCCC TCTCTGTGCG CTGGAGAGCT TACTGGGCAT CTTGCAGGTC 900 TCCTGGACAG AGGCCCCAGG GCTCAGAAGC ACACACACAC ATCCTGTCTA GTTTGTGGGA 960 CCCTGCAGAG CCCAGGCTCC AAGGGCTGCT GAGATGGCTC AGCACACGCG GGTCTGAGCA 1020 TCAAAGGCTT CTGTGCCTTG CGCCGCCCCC GACCCCGCCT GCAGCCTCAG CTGCCCTCTG 1080 CCTTCCTGGC AGGCACTGCC CATGGGTTCT CCGCCAGGGC CTGGCTGCTT TCCAGCCTGT 1140 GCCCCAGCCC CGGAGGGACC GTCCCCTGCA GATGACATGA GCTTTGCCTA AGGCCAGACT 1200 TGAGGACCAG TAACTAGGGA CAAAAAAATA GCTGCTCAGA ATAGCACAAA AGCTGTTGTT 1260 GTTCAGTTCT GAAAGTCTTA CTGCATCCTA TGGCCAGATG AAAAAGGAAC CGAGGCGGAG 1320 ACCCCGGGCA GGACGTGGTG CTTTTGCAGA CAGTAAGGGA ACCAGGCAGC CTCCAGCTCT 1380 GGTGTGCTCT CTGCCCGCAT GGGTCTGCAG CCCCTGCTCC CTCTCCTCAC CACGGGCTGC 1440 GAGCTCTTGG CATGGCTGCC CCAGCATCGG GGTTGCCCAG GTTTCCTGGC AAAAACCAAC 1500 TGAACGTTCA GATCACCTCC CTATTCAGCT GGCTTGGAGC AGAGAGCAGG AATGGTGCCT 1560 GGCCTCCTTC CCAGGCAGCC TTCCTGGGAA GCCTCCAGGG CCCTGGAAGT TGAGTGTCCG 1620 GTGCCTTCTT GTCTGTGGTC TCCTCTCTGT GATTCCCTGG GACATCCAAG GCCTGAAACA 1680 ATGTGGGGCT GAGGAAGCAA GGACGCCTTC GCCAGCCAGG CGGTCAGACA CCATGAGGTC 1740 CCAGGGAGGG GCTGTTCAGA CACCGACGGC CGAGGGACTC TTGTTTGCTT TATAAGAGAA 1800 TCCATCTTGT GAGCAGGGTG GGCTTGCAGG CAGTGGTTTT GTGTTTTTTT GAATTTCTAA 1860 GCTCAGTAGG TATGAGATGG 1880
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