Tag | Content |
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EnhancerAtlas ID | HS044-13371 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:80110560-80111660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr9:80111525-80111536 | TCTGCCAAGAA | - | 6.02 | Sox6 | MA0515.1 | chr9:80110715-80110725 | CCATTGTTTT | + | 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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| Number: 1 | ID | Chromosome | Start | End |
GH09I077495 | chr9 | 80110272 | 80111592 |
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Enhancer Sequence | GATTACATTC TCTAAAGTTT ACTGTATGCT TAAAACATTT TATAATAAGT AAGAAACCAG 60 AATGCTCCAC GCCTTCAGGA ACCCTGAGAA ATTCACTACA CACATAGTTT ACAGAAGGAA 120 GCAAATGAGA AGGAAAAAGT GTATACTAAG GGCTTCCATT GTTTTTTAAT GCTCTGTTTC 180 TTTAAAAACA AGTTGTTCTG AGCTAACCTA GCCAAACACT AAAGAAAGGC TACTTGCTCT 240 ATTAAACAAG TAAAATCATG TTCCTTAATT GGTCGGCTTT CTTCCCAGAG AGGATAATGT 300 TTCATGAGAG GAATGGAGAG TGTGTATGAT CCCAGGGAGG CCCTAGACTT GCTTGTAAGG 360 AATGGATCCC AAGAGAAGCA GGAGTGATGT CCGTGACAAG TTCCACACTG GGAGATGCAC 420 CGGGGGAGGT AGTCTGTCTA CATTGTCCTT GGAAACTTTT ACTGTATTCT CTGAAGATGA 480 GTAAATAGGG AAGGAATTTA CTGTTTTTCC TTCCTTTGGC AAATAATGAC ATTTCAGATA 540 ATGATAGTGG AAAAGTACTG TTTCTGAAAC AATTGTCTTT TAGGAAATTT TAATGTAATC 600 TGCCCATGTG GGGGAAGTAT TAACACTACC CAGGTTACTT CCACCTTGAC TGATTCATCT 660 CAAGCCTCAA GTACAAGAGC CAAGTTTTCA CAGGACATAA AATAGGAATT CTTTAACTCC 720 TTGTTACTAA GTACCTTCAA GAAGAGCTTT GCCCTACAAT GCCCTGTTTA TTCAGACTCA 780 AGATCCACAA AGTTTTAAGG ACAGCATAAA CTCCTCAGAT GGCACAAGCA CCTTCTGTAG 840 CCCAGATATA GGAGTGGCTG AGGGAAGGGA GAGGGCTCTC CCATCTAACT GCAAGGTCCA 900 GGGCTGTGGG TTGCCAGGTG CGCACAGTTA AACAAGACAA TGAAACAGGA GAGCTGTGAT 960 CTGGATCTGC CAAGAAAGAA GCACTAATCT GTATGGCAGG AATTCCTAGG TACATTCTTT 1020 CAGCCAAGAG GGAGAATCAG AGATGTCTGC ATGGAGGAAG TGACATTTGA ACTCGACCTT 1080 AGATTAACAA TGTACCTCTT 1100
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