Tag | Content |
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EnhancerAtlas ID | HS178-23033 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr9:4333800-4335340 |
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) |
RAX | MA0718.1 | chr9:4335324-4335334 | GCCAATTAAC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 4333911 | 4334927 | chr9 | 4334281 | 4334883 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I004334 | chr9 | 4334017 | 4334959 |
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Enhancer Sequence | TGGAAATATC CTCCCAAGAG AAATTATATT ATCATAAAGC TCCAAACAAC ACTTTACAAA 60 AAGGTGCGAT TTCAGGCAAC GCCAGGGAAA ACCACTTTGC ATTGGGAATT TCTTGGATTC 120 CTTAAATCCT ACCTGGAATG GTGCCACCTT GTCTGCTCTG ATGACCTCTG CAGGAGAGGA 180 AAGGACTAGG GTTCCTGTTA GGAGCTTAAG TGCTTAGAAA CAAAAGTGAC CTCTTCATGA 240 GGCAGACAAT ACTCTAGTCT CATAATTCAG AGGGCTTGAA TTTGAGTATC AAGACAAACA 300 GTTACAGCAA GTTCTGACTG AGCAGTGAGA TCTCATAAAA ATTCACCCAA ATTTAGGTAA 360 TAGGAATTGA TTCTACTACA GGTAAAGAAA CTGAGTAAAG GGGACAGTGA AAGACCATCT 420 GATAGTGTAA ATTCCAGGCA GGTTCTAAAT CTGTTTCCCA AGGAGCTTTC TGGATATAAC 480 ATTCAGTCCT TCTACAAATT ACAGAGAGAT CACAGAACCT CTCAAAACAA GCAACAATTA 540 AAACGTGGCA GCTACAGAGT ATGTGGGTAG ACAGAAAAGG TTGGCTGTCA AGGAGCTGGT 600 GGCTGGAGAG GCAAGGAAGC TGGTCAGTGC CCTCTGTCCC CTCCACCCTT CCTGAAACAA 660 TTGTAGTGCA AATGCATGTT CATTAATCAG CAAGTCCAAG CTAGGGCAGA CTTTTCTGGC 720 TCTGTTTGCA GTGCCAGGGC TCTTGCTCCA GCGTTGTCAT GGGGAAGTTA TTGTTGTCCT 780 CCTGGCAACA GGTTACCTAG GTGAACGCCA AACAGCCCAA CCTGGCCTAG TGAGCACTGG 840 GCCTGTTCAG CCACTGTCCC CATGCTGCTT TGCCTGTCTT CTCCTTATAC TCCCTCAATC 900 CACACTACTG CCCTTATGAG TCACAGCATT CATTCTCACA CACAAAGGTG CTACAGAAGG 960 CCACTTACAG CGAACCTGGG GCTTGTCCAA GGCCATTTTG TACTCTGACC TTTAAAAGCA 1020 TGCCCAGCCA TGGGCAGTCA TGCCTGCTCT CTTCAACCCA CAACTACAAT AAGAGCAGCT 1080 CTCAGAAGAG AAATCATTTC CACCTTTTTT TTTTTTTTTT TTTTTTGAAA CGGAGTCTTG 1140 CTCTGTCACC CAGGCTGGAG TGCAGTGGTG TGATCTCGGC TCACCGCAAG CTCCACCTCC 1200 CGGGTTCATG CCATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA GGCGCCCGCC 1260 ACTATACCTG GCTAATTTTT TGTGTTTTTA GTGGAGACGA GGTTTCACCA TGTTAGCCAG 1320 GATGGTCTTG ATCTCCTGAC CTCGTGATCC ACCCGCCTTG GCATCCCAAA GTGCTGGGAT 1380 TACAGGCATG AGCCACCGTA CCTGGCCCCA TTTCCACTCA TTTTTACTGA GCATCTTAGT 1440 GCCATAATTG AAACAAATTA GAAGCATAAG AAATAACTCC AGTGACGATC AAAGTCTATA 1500 CCACAAAGTG AAATGAAGCC CTAAGCCAAT TAACCTGTGA 1540
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