Tag | Content |
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EnhancerAtlas ID | HS098-19480 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr15:59174400-59175820 |
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 | chr15:59174414-59174432 | GGAATGAAGAAAGGTAAG | + | 6.07 | Nr5a2 | MA0505.1 | chr15:59174552-59174567 | TGTGACCTTGAATTC | - | 6.08 | TFAP4 | MA0691.1 | chr15:59175651-59175661 | ATCAGCTGTT | - | 6.02 |
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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 | AGAAATTTAT ACTAGGAATG AAGAAAGGTA AGGACAAGCC CCGTATTTCC AGTCAGGGTG 60 AATGAAATGG ATGGTGGCAC TATCAAATTG AAAGAAACTG GAGGCAACAA AAGGGACACA 120 AAGGTTTGAA AAAGGAGAGG AATGAGTTTG ACTGTGACCT TGAATTCATG GAAACAGCAA 180 AGCACTTACA TGGCAGTGGC AACATGAAGC TGAAAGGAAA CAGCAGTGTC TAAAGCTTAG 240 CCACGGGAAG GAGCCTGCAA AGGCAGTCAC AAAGGCAGAA AGAAAATGAT GGTGCCCTAG 300 AAAACAGACT CCCTCAAAAT AAAGATAAGT GACCGTGTGA AACAGTGTTT AACCACCAAG 360 GAGTCTGACA ACCATGAAAA TAAAAGAATC TATATTTATC AAGAGAAAAG TCATCGGTGA 420 CCTTTACAAA CCAGATACAA TGAATGTTGA GCTTGTGCAG GCAGAAGTAG CACACTTACT 480 GAAGTTTGAT GGTAGAAGTG ACCATGGAAT AGTAGTGACC TGGGTCACTG AGTCAAGCCA 540 ATAACTCTCC TAAGAAAGAG GAATGGGAAA GAAAGGAGGA CATGAAAGAG ATGGGGAAGC 600 TGAAGACCTG CTGGCTGAAG GGCCACATCC GACCTCAGTG TGAAGAGAAA GTAAAGCTCG 660 CCTCTTAACG TATGAAGAGA TTTTGTGTTA AATGTCTAAA AGCCTTCCCA AGAGTTATTT 720 TAAAAGGGAG GAAACAGAAC ACACTTTCAG TATTTTCTTC CTAAGAATTT GAGGAATGCT 780 AGGTAGAGAA CAAGATGATG GTTCCAATGT GAGGTTAAGA TTCATTATCT AGACTGAGTG 840 CAGTGGCTCC CGCCTGTAAT CTCAGCACTT TGGGAGGCCA AGGCAGGCGG ATCCCCTGAG 900 GTCAGGAGTT CGAGACCTGC CTGGGCAACA TGGTGAAACC CTGTCTCTAC TAAAAATATA 960 AAAATTAGCT GGGCATGGTG GCACATGCCT GTAATCCCAG CTACTTGGGA GGCTGAGATG 1020 AGAGAATTGC TTGAACCCAG GAGGCGGAGG TTGCAGTGAG CCAAGACCTC GCCACTGCAG 1080 TCCAGCATGG GCGACAGAGT GAGACTCCAT CTCAAAAAAC AAAAAACAAA ACAAAACAAA 1140 AGAATTCATT GTTTACTGGA TCCTGCCATA CGTACATACC CATATCTATA TCAACTTGCC 1200 AGAACGTCAC TGAATTCATT TAAAAGGAAG AATACAAACT AACACATTAA TATCAGCTGT 1260 TCTGCAAACA CTCTTTTGGA GACTACGGGT TGATACAGGG AAATGTTCAG GCAGATCTAG 1320 GGTTTTCAGT AGTTGCAATT CAGTCTCTCA GAAACTATAA TGACTTTTAT GGAAAGGATA 1380 AAGTGTTGGT TGTGTGCTGG CAGAAAAACT GGTTAGTTAT 1420
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