Tag | Content |
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EnhancerAtlas ID | HS052-39283 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr9:117565780-117567510 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:117565983-117566001 | CATTCCCTCCTTCCTTCT | - | 6.77 | Hnf4a | MA0114.3 | chr9:117566908-117566924 | AGGGTCAAAGTCTGAC | + | 6.29 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AATCCAGTCT TTTCCCATCT CCTCTGAGCC ATTTCTTCTC CATCAGTCCC TCCAGATCCT 60 CTCTCAGCCC TTCCTGACCC TGCTCTGTCC TGTGAAGCTG ACTCCTGGCT CAGTTGCCCC 120 TGGACCTTTG AGCTCTGGCT TCCTCCTGAG CCTGGTCAAT GGGATTGGAT TGGAGGCAGG 180 GTGGGGGATG GGGGAGCAGT CAGCATTCCC TCCTTCCTTC TGTGCTCTTG CTGCTGTTTT 240 GGCAGTGACT GCCTTTCTCC CCAGAGCCCT TAGGTCTTCC AGGCAGGCCC TCTCCTAGGC 300 TTTAGTTCTC TCTGGGTTTC TCTAACACTT CTCCCTCCAT GTGCCCTTCA TGCCAAGGCA 360 TGGTTGCTGG TTTCCCACTG TTGCTAGTGC TGGATGTTCC AGCCCTTTCA GTTCCCTTCA 420 ATCCGTCTGC ATCTCAGCAA AGAGGCCCTT CTTTAAATCC CTTCAAACTC TTTAAATATT 480 CTTCTACAAA TGCACTTTCT TGAGTGAGCC AGCTGTTTCT TTTCAGGACC CTGATTGCTA 540 CATGAGCCCA GCCTCACCCC CATTTCCCTC TCCTTTTCTT CTGACACACT AAGAAGTTAC 600 AGAGCCTGGG CAAACCAGAG CTGCAATCAT CCCCACACAT CTGCTCTCCA GGAAGATGAA 660 TTTAATGATA ATGGAATGGA TGGTGTCAGC CTTATTCATT TCTTGAGCAT CTGCAATTGG 720 ATAGGCACAG TGATAGATTC AGGTAGGGGC AGTAGCAGTG AGTAAAAAAG ACCCCGTGCC 780 TTCCTTCACC GAGCTTCCCG TCTAGTGACA GTGCATGTCT CCATCTCACC TTCTGGCTGG 840 GCAAGTCATG GATCCTCCCT GGTCTGTAAC ATTCTGCTTG CTGGTCTTCT AGATAGACAA 900 AGGCAGTCCT CGCCTTCTGC TGACCAAGGG CTCTCAGACA TCATCTTGAT CGTGGGAACC 960 TGTCATGCCT CTGGGCTTCC TTCAGACCCC AGTGCAGGTT TCTGGAGGCC ACTCAGTGTC 1020 TCATTCAAGG ACAACTATCT CCTTCTGGCT AAAGAGGGAC AGAGTCCCAG AGCACCAACT 1080 GGGCGCTGCA GTTTGACTTC CAGCAGAAAC TGGCCCCTTG GTGGTCAAAG GGTCAAAGTC 1140 TGACTTCCCA TGACCTGCGG TTCTTCTTTA ACATAAACAG CATTTCCGGT TTGTCTGCAT 1200 ATTTCTACAT TTTATGAGCA ATGGCATCTG GCCATGAACG CTGCTGCCTG AATCACAGTC 1260 TGTTTGTTGA CCCTGATGGG GCAGCGAGAA TTACAGATTT TCCATGGCTT ACTTGTGGTG 1320 TCTATGCTTT GAAACTGGCC AGGATTGCTT AGAGGCTAGG TTTCCAGTTA AACCCATTGA 1380 AAACCCATTT TTTTCCCTTT GCAATTTAAT ACTTTGAACT GAAATGAAAT CAGCCACCAT 1440 AGATTATGAA GGGACATTTT TAAAAAGGAT ATTACTGGAA AGACTCATTC CTTAGGTTTT 1500 GAGGTACATC TTTGTTGTTC CCAGCCAAGA ATTATGTTTT CTTCTTGACA CCTATCGCTG 1560 CCCCTACCAT TGTTCTCCCT AGACTTCATA TTCTTTTTCT GACTAGGCTT CTCCCAGGCC 1620 TCAGCAAGAC CTTAGAGATA GACAACCAGG CAGGAGGTTC TTTCTTAAGC TCTAAAAAGA 1680 GAAAAAGTTC TAAACCCAAG AAAAAGAGTG GGTAAAGAAA TTATAGCATC 1730
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