Tag | Content |
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EnhancerAtlas ID | HS098-23870 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:37270900-37272020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr17:37270970-37270981 | GACAGCTGCAG | + | 6.62 | NFE2L1 | MA0089.2 | chr17:37271540-37271555 | CAATGAGTCAGCAGA | + | 6.15 | Tcf12 | MA0521.1 | chr17:37270970-37270981 | GACAGCTGCAG | + | 6.14 |
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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 |
GH17I039114 | chr17 | 37270806 | 37271498 |
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Enhancer Sequence | GCTGCCTGTT TTACAGGTAC CACTACATAT TCTGAAGTCC AGGATAGGAT CATTTTACCA 60 AACAAAGCAG GACAGCTGCA GATGCTAAAC AGGTGCTCTC AGGTAAGTCT CAGAGTCAAC 120 TGAATACAGC TTCCACCTGG GAACCTGAGC GGGCCAGTGT TTAAGACGGT TGCTTTGAGG 180 CTCGGAGAAA GGTCTGGTTT CAATCAGCCT GCTTCCTGGG CCCCGCACAG CGAGAGCTTT 240 CCCCAAACCT CCGGGCGTCT GAAATGAGTG CCCGGGACAG AAGCCACGCT CTGCAGTTGT 300 GAAGCCCAAA CAGATGCTGA CGTGTCTCTT GCCGCCTCAG CTAAGACTGC AAAGCGTGAG 360 CTTCCTGGGA ATGCATCTTC CTGGCCCGTT GCTCGGAGTT CTCTGCTTCA CAGCAAAGAC 420 AAGCAGTCTG ATCCAAACTA GTGCTGTTCT GCAGAGAAAC CAGGCCCTGT GTCACGTGCC 480 TCAGCTCTGA CACCTGGATG ATCCCTGGAC TCATTCTTGG AGTTCCCGAT GACCCCTGCA 540 ATGGCACCTC TTAACTGACA GAAAACTTCC ATCTATTCTG ACTCAAGGAA AGTCAGAAAT 600 GAAACGAGCT GCTGCCTCTA ACTCCTAAGC TGATTCTCTC CAATGAGTCA GCAGATCCCA 660 GGGAAGGCAA GAGCCTCGAA GCCTAACGAT GCCCTACTCA GGCCAGCGAG GGTGAGGCCA 720 AGCTCTGCTT CAGGCCTCAG AAGTGCCAAG TACAGCTGGC CTGCCAGGGG GAGGACTGGC 780 TCAAGGGCAA TGCCATGCAG AATCTGCTGC AGGTCCCAAA CAGGCCCAAC AGACTGCCCT 840 CCTGGCACAC CTGACTTTTA TTACTCCAGG ACAGTGAAGC CAGGAGCCAT ATCTACTCAG 900 CTCTGGCTGA GGGTGGCCAC ACAGTGATGG GTGAGGCCAA ATTGCACCCT GGAGGGAGGG 960 GGCGACTTGC AGGGGGATCA CTCCTGGGCA GAGCCAAGCA CAAAGCCTGC AGGGGAGCAT 1020 TTGGGAGCGT GGGAGGAAGG AGAAGGGAAG CTGGCATTTG CTGAGTGGTG ATGGGAGAGT 1080 GCTGGGCATT TCATATTTGT TACTGCAGGG CAACCCTAGG 1120
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