Tag | Content |
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EnhancerAtlas ID | HS139-46385 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr6:15754300-15755440 |
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) |
EWSR1-FLI1 | MA0149.1 | chr6:15755056-15755074 | GGAAGAAATGAAGGTTGG | + | 6.15 | EWSR1-FLI1 | MA0149.1 | chr6:15755052-15755070 | GGAAGGAAGAAATGAAGG | + | 7.71 | Stat6 | MA0520.1 | chr6:15754817-15754832 | ACTTCTCAGGAAGTG | - | 7.63 |
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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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Enhancer Sequence | TTTGAAACAC AATTATAGGA GCTGGCTAAG CAGCCTCCCC AAGGCTGTTT CCTTGACTAA 60 TGTTTGAGCC TGAAGTCCAT GAGCAGGCAG GCAAGGAGAG CTGATGAGAG CAACCTAGAA 120 CCCCACGGGT TCTAGGCCAG ACTGAAACTC ATCCTTTTTT TTCCCTCTCA CCTTGATGAT 180 GAGGGTATCC TGCAGAAGTT GAGGCCCTGT GTCATGTTGC TGAACAAGTC ATCACCCACC 240 CCAGGGGTCA GAGAAGCTGT AGGAAGGTCC AGAGGGAAGG GAGGGCAGCG ACAGGCCCAA 300 CCACAGCTTC ATGTCAACGA GGTGAGTCAG CAGATCAGCA AAGCCTGTCC ATGTGCTGCA 360 AAATGGCTGT CCCTGCCATG CCTCCCTCCA TCTCTCATGA GAGAATAGCC CTCTAGCTCT 420 TCCTAACTGG AAACACAGGA GAAAGAATTC TGGGAAATGT AGTCTAGCCT AGCCAAGTTA 480 GCATATTCCA AAGCTCACTA AGGCTGTGGC TCTGCCCACT TCTCAGGAAG TGAGTTTGGT 540 CTTTAAACCA ATACCATGTG GCCTCCCGTT TCCCCAGCTG TTTTCTGCCT CTGCTGGCAG 600 AGCCGCTTGT GTTAGTCCAG GCCAAGGAGC AGACACCAAG CTAGATTACA TGTGCAAGAT 660 ATTTACTAGG GGAAACACCT ATGAAAGAAA ACAGGGAGGA AGCCGAGAAA AACTTGGAGA 720 GCTTTCATAC CATGATGCGA GTCCAACCTG GGGGAAGGAA GAAATGAAGG TTGGATAGAA 780 ACGACAGACT TCGATGCAAT TCTAAGGAAG GTTGGGCAAT GCTGCCTGTC AGAGCAGCCC 840 TGCTTTTCCC TGAGGCAGGT CTGTTTTAGC ATCCCGATGT GCTTAGGAGC AGCATTTGGG 900 AAGTGTGGCC TGCAGGAAAA CGCAGAGTTG CATTTCAGAG CACAGCGTTG GGGGCTCCTC 960 GATCAATTGC TCTCCCGGCA ATAGGAGGTC CAAAGGTGCC TTGTCCTGGC CATGCTGCCT 1020 CGTTCTCATT TCTTGCTTTG GTCAAAACTC AATCAGCCCA CCTTCCTCTT TTGGAGCATG 1080 AGAAGTAACT AACTAGGGCC AGGAGTCTTG CTGGCGCCTC TTTTGCCCAA TGCCTGATTT 1140
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