Tag | Content |
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EnhancerAtlas ID | HS044-03270 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:53882870-53883900 |
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) |
Foxd3 | MA0041.1 | chr12:53882937-53882949 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:53882941-53882953 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:53883105-53883117 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:53883109-53883121 | AAACAAACAAAC | - | 6.32 | MEF2C | MA0497.1 | chr12:53882924-53882939 | CTACCAAAAATAGAA | + | 6.43 |
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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 | AAAAAAAAAA AAAAAGTTTG AGACCAGCCT GGGCAACATG GCAAAACCCT GTCTCTACCA 60 AAAATAGAAA CAAACAAACA AACAAAAAAC AACAAAGCTG GGCATGGTGA TCCTGTGACT 120 GTGGTCCCAG CTCCTCTGGA GGCTGAGGTG AGATGATTGC TTGAGCCCAG GTGGCGGAGG 180 TTGCAGTAAG CCACTGAATC CCAGCCTGGG CGAAGTAGCC AAACCCCGTC TCAAAAAACA 240 AACAAACAAA CAAAAACCCT GAATCCTGAC TTGCTTCTGC CACATAATGG CTATGTGACC 300 TCAGGCGAGC TGTAGTTGAG CCTCAGCTAT ACAAAGGAAT AAACTGGCTG TCACTAAGGC 360 ACAGCAAACC CTTAATCCTA CACCAGACTT GTCCAGAACT TGGCCCCAGG CGCCATGCTG 420 GTCTCCCAAC TCACTCCACA CTTGTCAGTT ACCAGATCCT GAGATTTGAA GATTCCCAAG 480 AACAAGCATC CCTCTAATTG TTCCTCATAG CTAGCAGGGT CCTTCCATGA GCCCCTGGGT 540 TAGTCTGGAA ATGATTGCCA TACATTCTGA ATTGCAGTGG GGGAGGAGTG GCAGGAATCT 600 CTACATCTAG AAGGGTTCAG TAGATGATTA CACAGGCACA CAAGGAGGCT TGGGAAACTC 660 TGATAGTTCT TGTAATAATT ACCAGGCCTT TCCCTTGAAG ACTTTTTCCT GGGGGGTGAG 720 GGTGGTAGGC CTGGAATCAG CATATTTAAC AAGCACCCTA GATTTGTAAA GCTCTAACCC 780 AGTGCATGCT ATTTTCCAGT CCCACTGTTA CTGCCTTAGT TCAACCCTCA TTAGCTGTCC 840 TCACCTGGCC CAGGACAGCT GGTCTCCAAG TGCCCTCCCT AACCCCAATT CTCCACCCAG 900 CTCCTTCAGA AGGATCTTTC TAAAACAGAT TGGGGGCCAG GTGTGGTGGC TCATGCCTGT 960 AATACCAACA CTTTGGGAGG CTGAGGCAGG CGGACCACCT GAGGTCAGGA GTTTGAGACC 1020 AGACTGGCCA 1030
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