Tag | Content |
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EnhancerAtlas ID | HS147-21017 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr19:41885480-41886790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:41885553-41885571 | TGAAGGAAACAAGGAAAG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr19:41885493-41885511 | GGAAGGAAAGAAAGAAAA | + | 6.18 | EWSR1-FLI1 | MA0149.1 | chr19:41885545-41885563 | AGAAGGAATGAAGGAAAC | + | 6.33 | EWSR1-FLI1 | MA0149.1 | chr19:41885541-41885559 | AGAAAGAAGGAATGAAGG | + | 6.55 | EWSR1-FLI1 | MA0149.1 | chr19:41885549-41885567 | GGAATGAAGGAAACAAGG | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr19:41885530-41885548 | AGAAGGAAGGAAGAAAGA | + | 6.79 | EWSR1-FLI1 | MA0149.1 | chr19:41885526-41885544 | AGAAAGAAGGAAGGAAGA | + | 6.96 | EWSR1-FLI1 | MA0149.1 | chr19:41885489-41885507 | GGGAGGAAGGAAAGAAAG | + | 7.22 | EWSR1-FLI1 | MA0149.1 | chr19:41885481-41885499 | GGGAGGGAGGGAGGAAGG | + | 7.28 | EWSR1-FLI1 | MA0149.1 | chr19:41885600-41885618 | GAAAGAAAGGAAGGCAGG | + | 7.53 | EWSR1-FLI1 | MA0149.1 | chr19:41885485-41885503 | GGGAGGGAGGAAGGAAAG | + | 7.57 | EWSR1-FLI1 | MA0149.1 | chr19:41885604-41885622 | GAAAGGAAGGCAGGCAGG | + | 7.64 | EWSR1-FLI1 | MA0149.1 | chr19:41885578-41885596 | GGAAGGAAGGAAGGAGAA | + | 7.67 | EWSR1-FLI1 | MA0149.1 | chr19:41885566-41885584 | GAAAGGAAGGAGGGAAGG | + | 7.95 | EWSR1-FLI1 | MA0149.1 | chr19:41885574-41885592 | GGAGGGAAGGAAGGAAGG | + | 9.47 | EWSR1-FLI1 | MA0149.1 | chr19:41885570-41885588 | GGAAGGAGGGAAGGAAGG | + | 9.93 | Nr2f6(var.2) | MA0728.1 | chr19:41886463-41886478 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr19:41885575-41885596 | GAGGGAAGGAAGGAAGGAGAA | + | 6.15 | ZNF263 | MA0528.1 | chr19:41885531-41885552 | GAAGGAAGGAAGAAAGAAGGA | + | 6.25 | ZNF263 | MA0528.1 | chr19:41885490-41885511 | GGAGGAAGGAAAGAAAGAAAA | + | 6.51 | ZNF263 | MA0528.1 | chr19:41885483-41885504 | GAGGGAGGGAGGAAGGAAAGA | + | 6.58 | ZNF263 | MA0528.1 | chr19:41885567-41885588 | AAAGGAAGGAGGGAAGGAAGG | + | 6.71 | ZNF263 | MA0528.1 | chr19:41885487-41885508 | GAGGGAGGAAGGAAAGAAAGA | + | 7.06 | ZNF263 | MA0528.1 | chr19:41885571-41885592 | GAAGGAGGGAAGGAAGGAAGG | + | 8.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 41886054 | 41886513 | chr19 | 41885627 | 41885826 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I041380 | chr19 | 41885448 | 41886556 |
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Enhancer Sequence | AGGGAGGGAG GGAGGAAGGA AAGAAAGAAA AGAGAGAGAG AAAGAGAGAA AGAAGGAAGG 60 AAGAAAGAAG GAATGAAGGA AACAAGGAAA GGAAGGAGGG AAGGAAGGAA GGAGAAAGCA 120 GAAAGAAAGG AAGGCAGGCA GGCAACAATC ATGATGAACT CTTACGGTTT CTGTTGGTCA 180 GGAATTTGGG ACTTAGTTGC ATGGTTCTGC CTCTGGATCT TTCTTGAGGT TGCATTCAGC 240 TGGTGGGTGG AACTAGAACA GTCAGGGGCT GGCTGGGCAC TTTTCTCTCT CTTCATGGTG 300 TCTTAGGGCT TCCTTTTTTT TTTTTTTTTT TTTTTTGAGA TGGAGTTTCA CCCTTGTTGC 360 CCAGGCTGGA GTACAATGGT GCAATCTCAG CTCACTGCAA CCTCCGCCTC CTGGGTTCAA 420 GCAAATTCCC CTGCCTCAGC CTCCTGAGTA GCTGGATTTA CAGGCATGTG TCACCATGCC 480 CAGCTAATTT TGTATTTTTA GTAGAGACAG GGTTTCACTA TGTTGGTCAG GTTGGTCTCA 540 AACTCCTGAC CTCAGGTGAT CCACCCACCT CAGCCTCCCA GAGTGCCAGA TTACAGGCGT 600 GAGCCACCGT GCCCAGCCGA GTCTTAGGGC TTCTATGTGG TCTCTCCATG TTTGCTGCCT 660 TGGGATTCCT TACAGCATAA CGGCTTCAGG GCAGTCAGGC AGCTTATGTA CCTCCAGCCT 720 ACAGCATGAA TATTGCAGCA AAGCAGAAGC TGCCTCACCT TTTCTGATTT CGCTTTGGAA 780 GTCACGTAAC ATGACTTCCA CCACATTCTA TTAATTACAA GTGAGTCATG AGCCTGCTCA 840 AATTCAAGGG GAGGGGACAC AGAACTCATC CCTTGATGGG AAGGATATCA AAGTCACATG 900 GTAAGAAAAG CATGTGGGGC CGGGCGCTGT GGCTCATGCC TGTAATCCCA GCACTTTGGG 960 AGGCCAAGAC AAGTTAATTG CTTGAGGTCA GGAGTTCAAG ACCAGCCTGA CCAATGTAGG 1020 GAAAGCCCGT CTCTACTAAA AATACAAAAA TTAGGCCAGG CGCGGTGGCT CACGCCTGTA 1080 ATCCCAGCAC TTTGGGAGGC TGAGACGGGC GGATCACGAG GTCAGGAGTT CGAGACCAGC 1140 CTGGCCAACA TGGTGAAACC CAGTTTCTAC TAAAGAAAAA ATACAAAAAT TAGCCAGGTG 1200 TAGTGGTGCA CACCTGTAAT CCCAGCTATT CGGGAGGCTG AGGCAGGAGA ATCACTTAAA 1260 CCTGGGAGGC GGAGGTTGCA GTGAGCCGAG ATCACGCCAT TGCACTCCAG 1310
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