Tag | Content |
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EnhancerAtlas ID | HS139-57258 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr9:130179180-130180640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr9:130179951-130179962 | GGGGGCGTGGT | - | 6.14 | PLAG1 | MA0163.1 | chr9:130179991-130180005 | GAGGCCCTGGGGGG | + | 6.18 | SP3 | MA0746.2 | chr9:130179950-130179963 | AGGGGGCGTGGTG | - | 6.29 | SP8 | MA0747.1 | chr9:130179950-130179962 | AGGGGGCGTGGT | - | 6.52 |
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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 |
GH09I127416 | chr9 | 130179001 | 130181842 |
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Enhancer Sequence | CAAGGGGTGT ACATTGTCAA AGCTATTACA CCCCAGAAGG TTACACATGG GCTGTGTCTG 60 AAAGGGACCT ATTCCCTCAT CTCCAAATCA GTTATCAGGG AGTCCACACC ATGGACCAAG 120 GAAGAGGACC CGAGACAGGT TCATGCACAC ATTAGGTGTC TAATGACTGG GACAGCTGTT 180 TTGCTTGATA CCTCAGGCCA CACAGGGCTT GAGCAAGCAG CCTAACCTCC CTAAACTACA 240 GCCTCTGCTC GGGACACCCA CTCTCATCCA CCTCGCAGAA GACTGGTCTT TGTCCTGGAT 300 GAGTTCTCCA ACTGGGGCTT CAGGCCAGAG GCTGCTCCCA GCTCTGGCTT GGCTGTTCTC 360 CAGCCTCTGC AAAGCAGGGC TTGTAAAAAA AAGAGGGAAG GCAGGATGAT GTGTCAGCCC 420 CCAGGCTACA AGATAGATGG TAAACATGTG GGCAAGGAAC ATGTCACTGT GGCTTCAAAC 480 TCTTCCTCAG CCTCTCTCCT TTGCTCTCTG CTGGAGTCTG CATGGAGGGT AAGAGTGTGC 540 TTAGTTCCAA CTCTGGTTGT TCCACTCCCT GCCTATGTGA TGTGGACAAG TCACCTGACC 600 CCTCTCGGCC TGTTTCTTCA TCTGTCAAAT GGGCGTCATG GCACTACCTC CCTCATGGAG 660 TTGTGAGGAT GAAAGGCAAG AATTATGTAA AGCACCTGAA CCTGGGGACG GGACAGAGTG 720 AGTGCTCCGG CAATGGTCGC TGTTGTTACT GGTGCGAGTG AGGGTGGGGC AGGGGGCGTG 780 GTGAAGGTGG GGAGCTGTGC TAGGCGGGTG GGAGGCCCTG GGGGGGGTTC ATAAAGGGAC 840 ATTTGAGATC TTCAATCATT TTTCTCCTTA TATTCTATTT CCTACCTCGC CCTCTTGGCA 900 ACCCCCACCC ACACCACCTG CTGTTGCTAC CAGTACCCAC TTACCCGTGC CAATAATGTG 960 ATTCATACTC TTCAGAGGTC CCTTTGTTTC CCTTTAAGTC TTCCCATCAG AGCACAGAAT 1020 GCTTCGCGGA CCCAGAGCCA GCCCCCATTG ACCATCCTGT AGGGGCCCCA GAAGCCCAGC 1080 CTGGCGCCAT CAGTAAAGGA TTATGGAGAG GAGCACTGGA TAGAACAGCC CCAGGGGACA 1140 GGTGCAGCAT AAGCTTGCTT TACCCAGCCC AGGGCCGAAA TCTGCACGGC CCACGGACGC 1200 CCACTACCCC CTTACACCAT CCCAGCTCCT GCCCCAGAGT AACTTGGCTT CTGCAAACCA 1260 GAGAGACTTG TCCCTGATGC CCCCCGGGGA CCAGGGGTGG AAGTGCATCA GCTGGAGCAA 1320 GACACACTAG GCTACCTCAC GGTGGGCGTG TGCGGGATCC CAGGGCTAAG CCAGCAACCC 1380 TGTAGTGGCC ATTGGGGTTG GCACCTACTG AGCCTGGGGC TGCACGCAGA ATCGCACCAG 1440 CTGAGGTGTG ACGCTCTCTG 1460
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