Tag | Content |
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EnhancerAtlas ID | HS053-24354 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr20:44767580-44769150 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:44767908-44767926 | CTTTCCTGCCTCCCCTCC | - | 6.45 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGGGAATGA AGGGAGACCC AAGGGAAGGC ACCAGTGTTG GGGTTACTCA GGCAGCTTGG 60 GGCCACAGCT GTTTACCAGG AGGTTTGGAA GTAGTTCAAT ATTTTAACAA CCTCTGTAGT 120 AGGACTTCAT ATTCCAGCTG AGTTCCGATC TTGGAGCAGG GCGAGGGTTG GGGCTGCTTG 180 GTGCCCTCTC CCTCCTCTTT GCCCAGCAGT GTCTGGGATA TTCCCCACAA AGATCCTGCA 240 GGATGGCTGT GTCTCAGGCT GGTGCATCAG GGGCTGGCCT CAGAGCCAAA GGGTCCACAG 300 TGGACTTGCC AAGCCCAGAG TGCCAGAGCT TTCCTGCCTC CCCTCCCACT TTAGCCAGCT 360 CTCAGGGGGC CCCCCACCAC CCTGAGCACT GAGCTGGAAT TGGAGGCAGC CAGCCGGCTG 420 GGATGTGATC ATTCGGCCTC CTGAGCAAGG CCAGCCCTGG CCACAGGGAA ACAATGAGGT 480 CCCTTGAGTA GTCAAGGGTC TGCTGGGGCC ACTGGGCAGG ACAGGCCCTC CCTAGCCTGC 540 CCTGGTCTTG CTCTGGGACC TTGACCCTCT CCCCTTCTGA GGAAGGAGTA CAGTGGCTTT 600 GGGGGATGAT GAAGGCCAGA CAGCCAGACC CTCAGCACCT ATTGATGTTG CTGGCTGGGT 660 GGGTGTGTGT CTGAGTGCAG CCCCGGGCTC ACATTAGGTG GGGCGGGGGT GGAAGCCAGA 720 CATAGACTGC TCTGGAAATG AGATTTGCCT CGTTATCTGT GCTTGCTCAG ACCGAGGGCC 780 TTGGGCATTA GCCAGCCCAT CCAAGGAGTT AAGAAGCAGG AGGAGGGGCA GAGAGCCGAA 840 ATCCAGGCTC CAGTGGATAG AGCCCCTGCT GGAATGTGTG TGTATGTGTG TCCCTCGGTG 900 GTTTGGATTT GTGGGGTTTT GTCTACAAAA GTGTGTGTGT TTTCCTGGTT AGTGTGGATG 960 TCCTTTAAAA GAATGTGTGT ATAGCACTTT GCCTCCTGCT CATGGTGGTT GCTGTTTCTC 1020 TTTAGTGTGT GTGTGTGTGT TGCTGGAATT AACACAAGTA TGTCTGTTTC TGGACTGCAC 1080 CTGTGTGTGC ACACCCACAG GCTCCTGTTG GTTTTGTTTG TACATGCCCT GTTCGCATCC 1140 CAGCCCACTC AGAAGGCTGC AGGCCCAGAC ACAGCCTAAT GGACAGAGCC AGGTGGGCAG 1200 GGCAGGCTGG CTGGCCTGCA CCCAGGGGGC GGTGGGTGGA TCTGGGCATC TTCCAGAGGC 1260 ACCGGCCTGG CAGGGAACAA AGGGGCAATC AGTAGAGAGG CCACTAGAGC ACAGCTGATT 1320 GAGGAAGAGG AATTAACTAG GAGCCCCATG GGGCTCTGCA GGGGGCGGGG GCGGTGGCCC 1380 CTGGCATTCT GATTAGGAGG GGGAGCAGGT GCAGCTGGGC TTACCTGAGC CACAGGAAGG 1440 AGTTGGAGGG GGCAGAGGGG AAAGCCTAGG ATGGGATGAA GTAGAGCAGA GCTGGGAGCT 1500 GAGGACCTGG ACCAATGACT TTGAGGGAGA GGAGCAAGGG GTCCTGGGTG AGAAGGTCAC 1560 AGAGTGTACT 1570
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