Tag | Content |
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EnhancerAtlas ID | HS098-47797 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:15753960-15755500 |
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 | GAGTTTGGTA AAATCATGTT CCTCTCCCTC CTCACTTATG GGATAGGGTG GGTAGGGCCT 60 CTTTCCTCGG TTGTTATCTG AGCAGAGGAT AGTAATTCCA TCTTCCTTCA GTGCCAGGTG 120 GGCTGTGAAT GTGAACTTGT CCTCAAAATG CAGTTTCACC TTCCTGTTGT TGATGTCCAA 180 GTCTGAGGTA AAGCAGCGGA GCAGAGGGTT GGCACTGTGT GTGTTCTCTG TGAAGCCCAA 240 GGTGTACCAG TACCCTGACA TAAACTGGGG AAGGGGCACA CAATGAGTGT ATCATTCCGG 300 GTCCAAGCAG AGAAGAAGAT GGATATGTAT ATATAATTCA TTTGAAACAC AATTATAGGA 360 GCTGGCTAAG CAGCCTCCCC AAGGCTGTTT CCTTGACTAA TGTTTGAGCC TGAAGTCCAT 420 GAGCAGGCAG GCAAGGAGAG CTGATGAGAG CAACCTAGAA CCCCACGGGT TCTAGGCCAG 480 ACTGAAACTC ATCCTTTTTT TTCCCTCTCA CCTTGATGAT GAGGGTATCC TGCAGAAGTT 540 GAGGCCCTGT GTCATGTTGC TGAACAAGTC ATCACCCACC CCAGGGGTCA GAGAAGCTGT 600 AGGAAGGTCC AGAGGGAAGG GAGGGCAGCG ACAGGCCCAA CCACAGCTTC ATGTCAACGA 660 GGTGAGTCAG CAGATCAGCA AAGCCTGTCC ATGTGCTGCA AAATGGCTGT CCCTGCCATG 720 CCTCCCTCCA TCTCTCATGA GAGAATAGCC CTCTAGCTCT TCCTAACTGG AAACACAGGA 780 GAAAGAATTC TGGGAAATGT AGTCTAGCCT AGCCAAGTTA GCATATTCCA AAGCTCACTA 840 AGGCTGTGGC TCTGCCCACT TCTCAGGAAG TGAGTTTGGT CTTTAAACCA ATACCATGTG 900 GCCTCCCGTT TCCCCAGCTG TTTTCTGCCT CTGCTGGCAG AGCCGCTTGT GTTAGTCCAG 960 GCCAAGGAGC AGACACCAAG CTAGATTACA TGTGCAAGAT ATTTACTAGG GGAAACACCT 1020 ATGAAAGAAA ACAGGGAGGA AGCCGAGAAA AACTTGGAGA GCTTTCATAC CATGATGCGA 1080 GTCCAACCTG GGGGAAGGAA GAAATGAAGG TTGGATAGAA ACGACAGACT TCGATGCAAT 1140 TCTAAGGAAG GTTGGGCAAT GCTGCCTGTC AGAGCAGCCC TGCTTTTCCC TGAGGCAGGT 1200 CTGTTTTAGC ATCCCGATGT GCTTAGGAGC AGCATTTGGG AAGTGTGGCC TGCAGGAAAA 1260 CGCAGAGTTG CATTTCAGAG CACAGCGTTG GGGGCTCCTC GATCAATTGC TCTCCCGGCA 1320 ATAGGAGGTC CAAAGGTGCC TTGTCCTGGC CATGCTGCCT CGTTCTCATT TCTTGCTTTG 1380 GTCAAAACTC AATCAGCCCA CCTTCCTCTT TTGGAGCATG AGAAGTAACT AACTAGGGCC 1440 AGGAGTCTTG CTGGCGCCTC TTTTGCCCAA TGCCTGATTT CTGTTCAATC AGGATAAGCT 1500 GTCAGGAGGA GATGGTGGCC ATACTTGGAG GTGAAGGGAA 1540
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