Tag | Content |
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EnhancerAtlas ID | HS139-46727 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr6:30186270-30187680 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr6:30187110-30187129 | TTGTCAGTAGAGGGCACTG | + | 6.18 | Foxd3 | MA0041.1 | chr6:30186577-30186589 | GTTTGTTTGTTT | + | 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 |
GH06I030219 | chr6 | 30187061 | 30187377 |
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Enhancer Sequence | TTATCCCATA GAATGTTCCC AGTACTGGAT TTGGTTGATT GCTTCCTCAT GGTATCAATT 60 AACTTGTTCC TCTATTTCCT GTGTATCTTA GATAAGATTC ATAAGATAAT AAAGGATGCT 120 ATGTAGTCAT CTCTCATTCT AAGCAATCAA ACATTTTCAA TATCTTTCAC CATATGTCCC 180 TAACCCAGAT ACTACTAGTC CGTCTCTCTC TGCTATAGAG GTAAGCATCA CTCTGCATTT 240 CTGTGATAAT CATTCCTTAG CTTTTATTTT TATTTACTTA AAAGGCTTTA TCAGATTTGG 300 GGTTTTTGTT TGTTTGTTTT TGAGATGGAG TCTCGCTGTC ATCCAGGCTG GAGTGCAGTG 360 GTGCAATCTC GGGTCACTGC AACCTCTGCC TCCTGGGTTC AAGTGATTCT CCTGCCTCAG 420 TCTCCTGAGT AGCTAAGATT ACAGGTGCCC GCCGCTATGC CAGGCTAATT TTTGTATTTT 480 TAGTAGAAAC GGGGTTTCAC AATGTTGGAC CAGGCTGGTC TCAAACTCCT GACCTCAGGT 540 GACTCGCCTG TTTCGGCCTC CCAAAGTGCT GGGATTGCAG GCGTAAGCCA CCACTCCCGG 600 CTGGGTTCAA TTTTTTAAGG AGAATACTTC AAAAGCAGTG CTGTGTACCT ATGGTATCAC 660 ATTTAGAGGT ATATGATCTC ATCCCACTAT TAGTGATGGT AGATTTGATG GAAGATTCAG 720 GTATTGTCAG CCTGATCCCT CCATTCCCCA GTTTGTGAGT TATGGATTTA CTGCCTCTCA 780 GCTCCAAAAA TGATCCTGAA TCTTTTAATT ATGTTTTCTT TGCCATCTGG CCCTGAAGCT 840 TTGTCAGTAG AGGGCACTGG AGAGTCATTG CAGGGAAAAA CGATTTTGCT TCCTGGTTCT 900 GGTGTGCTGT TTGCCAGGTT CCTGCAGTGA GTGCATGGTT TAGCAGCACC TGCTCCTGCA 960 GCACCCAAAA CTTACCTAGT GTCCAGTTAC TTCAGTCACA GTCAGCAACA CCCAGCAGTG 1020 AGCAGCTTCC TTAGGCACCC CTCCTGAAGG GGTTTTATAC TGGAGTGTCT CTGGTATGAA 1080 CAGCTTTTGC CTGCACCCTA GAGAGTGGGT TTCCAGCAAG TTCTGCCATA GCAGAACCAC 1140 CTTGATGTCT CTACTCTCCC TGAGAAGGCT AGATCCCATC CTCTCTTGTT TTCTCAAAAA 1200 TGGACTAACC ATCTATAAAT ATCTACTCTC CTGCTTCAGC AAATTTTTTT TACCGTTTCA 1260 CTGAATTATT CTCATGAGCA TACAAACATG TTATAATATA TCGCTTTAAA AACCAAAACA 1320 AGACAAACTC CTTGATACCA TAAGTTTTTT TGTTTTTGTT TTTGTTTTGT AGAGTTTTGC 1380 TCTTGTTACC CAGGCTGGAA AGCAATGGCA 1410
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