Tag | Content |
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EnhancerAtlas ID | HS047-34198 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr9:88215160-88216370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:88215442-88215460 | AGAGGGAAGGCAGGCAGG | + | 6.26 | YY1 | MA0095.2 | chr9:88215292-88215304 | CAAGATGGCTGA | + | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 88215373 | 88216332 | chr9 | 88215488 | 88216200 |
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| Number: 2 | ID | Chromosome | Start | End |
GH09I085600 | chr9 | 88215661 | 88215810 | GH09I085601 | chr9 | 88215981 | 88216170 |
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Enhancer Sequence | TGATCCCTTC CTGGGACTCA GTGAGCCACT TCAATCTGAA GTTTTGACCC CTCCACTCAC 60 ATAAAACTCA CCATAACACA AAACTCATTA TAATAGTTTC AACAGTGACT ACAGGAGACA 120 GAGGAGGGGC TTCAAGATGG CTGACTAGAG GCATCTGGCA CTTACGTCCT CCACAAAGCA 180 GCAGCAAAAC AGTGAGTAGA TAACCACACT TAAAATAGAT CATCTAAGAC AGAACACTGA 240 AACTCAACAG AGAAGTAACA AGAACACCTA AGACAAGGAA GGAGAGGGAA GGCAGGCAGG 300 CTACTTGGCC AGGAGACCAG GGAGGCTTCC CAGTACAGGA AAAGGGTAAG TGAGATTCTC 360 AGTGGTCCAC ATCCGCACTA CAGACTCCTC CAATCCTAGC CAGGGGGGAG CCCTCCATCC 420 TCACAGGTCC CAAGACTAAC ACAGGGAGCT GCTTCGAGAC TGCACAAAGG TATTGCTCCA 480 GAGAGTGAAC TCACACGGGG TGTGACCTAA GCAGCAGCAG CATTGGCACA GTTTTGAGAA 540 CCCAGCCCCC ACTCAACTGC ATCCTGCCCC GAGGCCCAAC AGCCTCTGCC TCCCCAACCC 600 ACAGCCACCA ATGCCACAAG CTGCTGCCAC TGAAACCTAA GCAACAGTCA CTGGCAGAGA 660 CCCCACTTCC CAGCAGCAAG CTGTCATGCA TTTGCACGTG CCCAGAGGAC AGGGTCCCCT 720 ACCCACAGCC ACCACCACTG CTGATTGCTG TCACTGGGGC CAAAGCACAA TTCCCTGGTA 780 GCAACTCCAT TGCCCTTATT GCCCTTGGCA GTGTGGTCAC CCTATATTAA CACACGCCTT 840 GCAAACAGGC TCCCAGGTCC CCAGCTGTCG CCTGGGGCTG AGGCACACAT TCCCCAGCCA 900 CTCGCCTACA GCTGCTGCCA CTGATAGCTG CATAGCAATC CCTAGCAGCA GGGCTGAGGT 960 GCATTTGCAA GCGCCCTGGG GGCAGGCAGA CTTCCCCAGC CCACCAGCAC TGCTGCTGCC 1020 CTCACTCAAA CACTCTAAGG GGAGCCTAGG GATCACCCAG CCGTCCTCAT TATAGCCAGA 1080 GCCCCTGTAA ATCACGTGAG GGGCTTGAGG ACAGGCCTGC CTGGCCTGGC TCCCCCACCA 1140 TCCCCAATAC CAGAGCATAC CTGGGAGCCT AGGGATCACT CAGCCATGTC AACCAGCGCT 1200 GGCACCTGAG 1210
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