Tag | Content |
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EnhancerAtlas ID | HS116-14707 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr17:37252450-37253860 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:37252604-37252622 | GAAAAGAGGGAAGGATGG | + | 6.23 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 37252674 | 37253297 | chr17 | 37252696 | 37253783 |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I039092 | chr17 | 37248266 | 37253899 |
| Enhancer Sequence | ATAATCACGA GTGGAGCCCC AGCAGGGGAC CCTGCCCCAC GGGGGAGAAG TAGGGGGGTC 60 CCTCAGCATT GAAGCAAAGC AGAAAAAGGC AGAGAAAGAA GAGGCCAGAA ATGACTCAGG 120 GAGCAGAGTA GTGGGAAAAA CAGAAGTGAG AAGGGAAAAG AGGGAAGGAT GGGCCCCCAG 180 ATGGATTAAA AACTTCCAAC GAAGGGCACT TTAAAGGATC CTTTATCAGA AAAGGCAAAA 240 TTGGCCAGAT CCTCAGCTTC TCCCTGCACC CACTTCCTCA CGTGGCTGCC CCTAGATCCC 300 TTCTGTAGCC TGCTCTGGGA CCCACCCCTC CCTTACCTGC AGCCTGGCAG GAAGGTACAC 360 ACAGCTCAGG CCCTGACATA TATCTGGACT CAAGTCTGCC TCGGAAAGGA CAGGAAAGTT 420 CCGGTAAAGG AGGAGGACCA GCATGTTGGG GCCGTCCAAG GCCATTCGGG GCCAGCCAAG 480 GGGCAGGCTA CATTCTGGAG CTCTTTGTAA GAAAATCCTC ACTAACTGAT CCCACTAATT 540 CAGAATCCCT GTCAGTTTCG ATGTTGGCAA TGCTAAAGTT GCTTTTATAC TAACCATGAA 600 ATAAAGAGTT TCTTAAGCAA ATGAACAGAG GAAATAATAT TGACTTCCGG CGGTCTCCCC 660 AGCCACATAG CGGATACACT GTCCTGTGTG TTTTGAGTGC CTCTGCAAAC AGATGCTGCT 720 AATTGCACAT GACTTTTCTT TTCACCAAAG ATGCTTTGCA GACTCTGCTG AAAAGCCTGC 780 GGAAGAGTTT ATACGAGGAA GTACTGGTAA GAACTCTTGT GGTTTTCAGC CTCTTCTACC 840 CTCTCCCCCA GGAGTGAGGC TGTGAGGAGT CCTCCCCATT GCACCTCCCA TCCCCTTGCC 900 TAGCAGGGGT GGGGAGGAAA GTGTTTAGAA CCTGGGGGAG GAGAGTTTTC CCCAGACAGG 960 GTTCAGTGGC TGGGGATTCC TAAATAGTGA GGAATCAAAC TCCCCTCCTC ACACTGCCCC 1020 AGGCAGGGAG CAGTCAAACC TGGGCACAAG GACAGTGACG CCACCCATTC TGTATGATCA 1080 GGTGGGCTTG GTCAATAGGA TTATCCATGG TGATCATAGG GTCTGCAGAC CAGATGGCTC 1140 TTCCTGAACT TCTGTTTCCT TTAAGCCATG ATCATTTGGG GTTTACTATT ACCTGCAGCT 1200 CAACCTAATC CAAACAAATT CCCTGCTTGC CGGATTGAAT GTGAGACCCA AAGTCATCTG 1260 ACCCCTTAGC CACATAAAAG CCATTTCTCC CCAGGAGCAG AGGCTGTGGC CCATTTTAAA 1320 CCCCAATGAG GGCCATGGAT ACTGTCCCAG AAAAACGCAT GGATGTGAAC ATGTTCCACT 1380 TGCATTTCAA TACTCCACAT ACAGGCCTTA 1410
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