Tag | Content |
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EnhancerAtlas ID | HS098-23657 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:28570760-28572340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr17:28571719-28571730 | CTGCAGCTGTT | - | 6.02 | SOX10 | MA0442.2 | chr17:28571701-28571712 | AAAACAAAGAC | + | 6.14 | Tcf12 | MA0521.1 | chr17:28571719-28571730 | CTGCAGCTGTT | - | 6.62 | Zfx | MA0146.2 | chr17:28571441-28571455 | GAGGCCTAGGCGGG | - | 6.24 |
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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 |
GH17I030244 | chr17 | 28571847 | 28572386 |
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Enhancer Sequence | CCTTGACACT GAAGGCGTGA CCCGAATGAG AAGCCAGCCA TGCAAAGACC TGAGGGAAGA 60 GCTTTAGGTA GACGGAACAG CAAGGAGGAA CAGCAAGGAG GCGGAGATGA GTTTGATGTG 120 TCTGAGGGAC AAAGTGCGGG ACAGGGTGGG AGGCGGTCAG TGGCTGGCTG AAGCAGAGTG 180 TACAAGAAGG GGAGTAAGTC GAGTCTGGAG AGGTGGGCAG GGGCCACAGT GAGAGGCTGT 240 GTGTTCCTGT CAATGTGTGC AAATAGAACT TAAAAGACTT ACTCGTTTTG GAGAATTTTG 300 GACTAGGTTA ACCCATAAGG TCTCCGCCAG GTGAGATGCA GGGATGCTGC TATGCTAAGT 360 CAAGCACCCT CCCATACTCT CCATCAAATA GCCACCCTGC CTTGGCTGCC CTAGCCTTCT 420 GCACAGCAGC TGATTTTTAA AAAACAAACA GCTGTCATGG GGTAACCTGA AAGATGGCTC 480 CAGAACTCAT TCTGTCCACT TCAAGACGTG CTACCAAACT AGAGTTTTTC CAGAGGAGTC 540 AGCAAGAGGG AAAGCACTGA GTATTCAAAC AATATCCAGG AAAGATGATG TGGAGGGTTT 600 CCCATCTGCA CACAATCCTC TTTCCAAATA GCTACAGCTA GCCAGACGCA GTGGCTCACA 660 CTTGTAATAC CAGCACTTTG GGAGGCCTAG GCGGGCAGAT CAATTGAGGC CAGGAGTTCA 720 AGACCAGCCT GGCCAACATG GCAAAACCTT GTCTATACTA AAAATACAAA AAAAAAAAAA 780 AAATTAGCTG TGGTGGCGCA TGTCTGTAAT CCCAGCTACT CTGGAGGCTA AGGTGGGAGA 840 ATTGCTTGAA CCCACGAAGT GGAGGCTGCA GTGAGCCGAG ATCGTGCCAC TGTACTCTGC 900 ACTCCAGCTT GGGTGACAGA ATGAGACTCA AAAGAAAAGA CAAAACAAAG ACCAAATAGC 960 TGCAGCTGTT GTGAATTGAA CATTCCCCTA TTTCCTTTCC CTCTGCAATA ATGTGTAAAG 1020 GACTTGGAGT TTGAAAAAGA AAAACAGAAA AACCCGGCCA GTTTAATCCT AGTTTTCAAC 1080 CCATTTGTGT CACAGACCCC AAGAAGGAAG CCATTGGCTT CATGAGTATC AACAACAGTT 1140 CTCAACAAGT TGTCCTAAAT ATGACCACGC TCATCTGGAA TCACTTTAAA AAGTATCTAA 1200 CTTAACAAAT GACTAACTAG AGCCACCGTG GGCAATGGTG CTCACCCACA CCACACTAGA 1260 GGAATAGGAC TTCAAGTCCA AGTGCCCTGG TGCCACCAAC AGCAACTTAG AATTAAGCTG 1320 CTCTTTAAGG ACAAGCCAAA GCAAGCAGAT GGGCCACACC ACATCCTGAA GGCATGTCTC 1380 ATTATCATGC CTTGGCTTCT TGGACGTGTA GGGTCACCAT TACTCAGGCC AGGACTTCCC 1440 AGAGGCCAGT CATGAAGCTC TCCTCTGGTG ACACTGTATG ATTCACAGTT AAAGCAAAAG 1500 ACAACTCCAT GCCTTCCCAT TTCCTACCTC ATTCGTCACC CAAATACTAG CAGTTTCTTC 1560 CAACTGAGAC CTCCAGCTAC 1580
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