Tag | Content |
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EnhancerAtlas ID | HS098-38419 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:45388020-45389630 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr3:45388031-45388044 | TTCTAGAATCTTC | + | 6.78 | ZNF740 | MA0753.2 | chr3:45388056-45388069 | CTGCCCCCCCCAT | + | 6.36 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH03I045346 | chr3 | 45387972 | 45388078 |
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Enhancer Sequence | CATACTGCTG GTTCTAGAAT CTTCCAGGTC ATTGTACTGC CCCCCCCATC TCCATCCCTA 60 CCCCAACAAT TAGTCCAGAG CCTTCTTTTT TTTTTTTTTT TTTTTTTTTA GACGGAGTCT 120 CACTCTGTTG CCCAGGCTGG AGTGCGGTGG CGCAATCTCG GCTCACTGCA AGCTCCACCT 180 CCCGGGTTCA TGCCATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGACTA CAGGTGCCCA 240 CCACCACGCC CAGCTAACTT TTTGTATTTT TAGTAAAGAT GGGGGTTTCA CCATGTTAGC 300 CAGGATGGTC TCCATCTCCT GACCTCATGA TCTGCCAGCC TTGGCCTCCC AAGGTGCTGG 360 GATTACAGGC GTGAGCCACC GCTCCCGGCC AAGCCCAGAG CCTTCTGTAG TCAGATGTAT 420 CTAGGGAAAC TCATCTGATT TGAATCCAGC AGGCAATATT CCATCTAATT AAGCAATTAG 480 GAGCAGGAAG GCAACATCTC TGGAGCCTAC CTGAGTTCTG TAATGAGCCT TTATAAACCA 540 CACTGGTTGT TGTGACAGAT GCTGGGGTCT GCCGAGATCT CTGGACGCAG AGTTTTGCTG 600 AGTCCCAGTG GGGGCTGTGG CTGTGGCTGT TTATAGAATC TGAGGTCTGC ATTTGGATAA 660 TTACCTCCAT GTGATTATCA GATTAATGTT ACCTGGGCTA GAAGGTGTTT TTGCTTAAGG 720 GAAGAAAAAC AAAACCCTTT GAGGATGCCC AGTGATTGTG AACTTGAAAA GAGCCTGATC 780 CTTAAAAGGT AGTGAACCAG TGTGGTGAGG CCAGACTACA GCCCCACAGT CAAGGCCAGC 840 AGGTGTGCCA TAGACACACA GGCCAGCAAA CATACATGCC AAGAAAGTGT GTCTGTCGAT 900 GAGGTAGGGA AGAGCCTGAA TGAAAATGTG TTCATTTTCC TACTTCCCTC ACACACGCAT 960 ACACTTAAAC ACACCCACAC ACATGCACTG CAAATTCACT GAGAAGCAGG GAGCAGCAGG 1020 GCTTCTGATC AGCACCCTCT AACACAGGTG ACTTCTGTCA GGAAAGATTC AGGCTGGAAA 1080 ATTCAGGAAG AGGACAGCTT GGGAAAAGGC TGGTCCCAAT AGGAGCTACT TCCATCTTGG 1140 ACACTGGAGC CACTGCTGTT GTTGTTACCT AAGGGTCAGA CATTCAGCTC AAATTCACAG 1200 GCAGAAATAT TTCAGCACCA AGACAAATAT CTTTCTCTCA GAGGAATTCC TCAAAGACGT 1260 TTATGCTGCT GGGAAAGATG CCACTGGTCA TGTGCCTGCC ACTCAGCCTG ACAAAAACGC 1320 TGGTCTGTGG GTAGGAGGCA TCCAGTAGAT GCTACAGAAC AGTGTTTTCC CTCAAGGCCA 1380 ATGGAGGGGG ATGAAGTCCT CGGGTGGCAC CTTGTGGGCA GGTCTAGGGG TTTGTATGCT 1440 TTTTTTTTTT TTTTTGAGGC AGAGTTTTGC TCTTGTCACC CAGGCTGGAG TGCAATGGCA 1500 CGATTTTGAT GCACTGCAAC CTCCGCCTCC CAGGTTCAGA TGATTCTCCT GAGCCTCCCA 1560 AGTAGCTGGG ATTACAGGCA CCCACTACCA CACCCAGCTA TTTTTTGTAT 1610
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