Tag | Content |
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EnhancerAtlas ID | HS180-20530 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr17:37252400-37253650 | 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: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I039092 | chr17 | 37248266 | 37253899 |
| Enhancer Sequence | AAAGTCTTCA TGCATTCTTT TGTTCCTTGG CTCATGTGAT TATTCATTCA ATAATCACGA 60 GTGGAGCCCC AGCAGGGGAC CCTGCCCCAC GGGGGAGAAG TAGGGGGGTC CCTCAGCATT 120 GAAGCAAAGC AGAAAAAGGC AGAGAAAGAA GAGGCCAGAA ATGACTCAGG GAGCAGAGTA 180 GTGGGAAAAA CAGAAGTGAG AAGGGAAAAG AGGGAAGGAT GGGCCCCCAG ATGGATTAAA 240 AACTTCCAAC GAAGGGCACT TTAAAGGATC CTTTATCAGA AAAGGCAAAA TTGGCCAGAT 300 CCTCAGCTTC TCCCTGCACC CACTTCCTCA CGTGGCTGCC CCTAGATCCC TTCTGTAGCC 360 TGCTCTGGGA CCCACCCCTC CCTTACCTGC AGCCTGGCAG GAAGGTACAC ACAGCTCAGG 420 CCCTGACATA TATCTGGACT CAAGTCTGCC TCGGAAAGGA CAGGAAAGTT CCGGTAAAGG 480 AGGAGGACCA GCATGTTGGG GCCGTCCAAG GCCATTCGGG GCCAGCCAAG GGGCAGGCTA 540 CATTCTGGAG CTCTTTGTAA GAAAATCCTC ACTAACTGAT CCCACTAATT CAGAATCCCT 600 GTCAGTTTCG ATGTTGGCAA TGCTAAAGTT GCTTTTATAC TAACCATGAA ATAAAGAGTT 660 TCTTAAGCAA ATGAACAGAG GAAATAATAT TGACTTCCGG CGGTCTCCCC AGCCACATAG 720 CGGATACACT GTCCTGTGTG TTTTGAGTGC CTCTGCAAAC AGATGCTGCT AATTGCACAT 780 GACTTTTCTT TTCACCAAAG ATGCTTTGCA GACTCTGCTG AAAAGCCTGC GGAAGAGTTT 840 ATACGAGGAA GTACTGGTAA GAACTCTTGT GGTTTTCAGC CTCTTCTACC CTCTCCCCCA 900 GGAGTGAGGC TGTGAGGAGT CCTCCCCATT GCACCTCCCA TCCCCTTGCC TAGCAGGGGT 960 GGGGAGGAAA GTGTTTAGAA CCTGGGGGAG GAGAGTTTTC CCCAGACAGG GTTCAGTGGC 1020 TGGGGATTCC TAAATAGTGA GGAATCAAAC TCCCCTCCTC ACACTGCCCC AGGCAGGGAG 1080 CAGTCAAACC TGGGCACAAG GACAGTGACG CCACCCATTC TGTATGATCA GGTGGGCTTG 1140 GTCAATAGGA TTATCCATGG TGATCATAGG GTCTGCAGAC CAGATGGCTC TTCCTGAACT 1200 TCTGTTTCCT TTAAGCCATG ATCATTTGGG GTTTACTATT ACCTGCAGCT 1250
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