Tag | Content |
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EnhancerAtlas ID | HS044-02950 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:360870-362600 |
Target genes | |
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) |
EWSR1-FLI1 | MA0149.1 | chr12:361833-361851 | GGAAGGAAAACAGGAAAG | + | 6.27 | HNF4G | MA0484.1 | chr12:362055-362070 | GAGGGACAAAGTCCA | + | 6.22 | Hnf4a | MA0114.3 | chr12:362056-362072 | AGGGACAAAGTCCACA | + | 6.6 | Nr2f6(var.2) | MA0728.1 | chr12:361047-361062 | GAGCTCAGAAGGTCA | + | 6.1 | RARA | MA0729.1 | chr12:361047-361065 | GAGCTCAGAAGGTCAAGG | + | 7.13 |
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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 | CACTTTGGGA GGCCAAGGCT GGAGGATCGC TTGAGCCCAG GAGTTTGAGA TCAGCCTAGG 60 CAACATAGTG AGACCTCGTC TCTACCAAAA AAAAAAAAAG TTTTTAATTT TCCGGGCATG 120 GTGGCACATG CCTATAGTCG CAGCTACTTT TGGGAGGCTG TGGTGGGAAG ATCATTTGAG 180 CTCAGAAGGT CAAGGATGCA GTGAGCCGTG ACTGCACCAT TGCACTGCAC CATTGCACTT 240 CGGCCTGGGT GACAGAGTGA GATCCCATCT CAAAAAAAAG AAAAGGAAAA TTACAAAACA 300 CAGAATGAAA AAAATAGTAT TTGTAAAATG CATTTCTGAT AAAGGACTTG TGTGTTAGAA 360 TATATGAAGA TACCTCGATA ACAAAGGATA AACTACTGAT ACATGAAAAC TATAAATGAA 420 ACCCTAAATA ATTATGCTGT ATCATAATTA TCAACATACC ATATGATTCC ATTTATATAA 480 TATTCTAAGA AACGCAAACT AAGGTATGGT GGTATCACAA TTTTCATAAT TATCAACACA 540 CTGTATGATT CCATCTATAT AATATTCTAA GAAAAACAAA CTAGTTTAGT TTGCATTTAG 600 CATAATTATT GATTGCACTG GGATGTGATG GCAGGAGTGA AGTTGGGAGG AAGGAATTAG 660 AAAGAGACAG GAGTAACTGT TTTGGAAGTG ATGGACATGT TTACTATCTC AATTGTGGCA 720 GTGGTTTCAT GCGTATATAC ATATGTCAAA ATTTATCAAA TTGTACACTT TAACTATGTG 780 TGGTTTATTG TAAGTTAATG AGGAACCCAG TTCTCCAGTT CTTCACCTCC CACTTCTCAA 840 GGTTGTATTC TACACATCCA TAATTCAGGC ACTAAGGGGG ACTTGATCAT GAGGACAAAG 900 AAGGAAAGGT AGCAAACAAT TCAGCCAAAG AAGTCCATAA ATCAACCCAA GGTTTGCTGA 960 GCAGGAAGGA AAACAGGAAA GATAGAACCC AGCAGCTGAC AGGAACAGTC ACTGTGGAGA 1020 GCCCAGTCCA GAAAGAAACA GCTATGGGCC CAGCCCAAGC CCCTTCCCAT ATTCATGCTT 1080 CCTGCTCTTT CTCTATAAAC CAAGCCAATG TTTAACTCTG GGCCCCGTGG TCAGCTGCTC 1140 CCACCTCCTT CCTCTGCCTC GTTGAGCTCC TTGGCAGCCT GCCAAGAGGG ACAAAGTCCA 1200 CACCTGCAAG GAGGGGCTAC AGGCCCTAGA AGTGTGAGAG GGGTCGGGGT GGGAGGGAGC 1260 CAAGGGGGCC AGGTACGGAC TGAGGAGTGC TGAAGGGCAT TCTGCCTCTT CCCCTCCGCA 1320 GGTACCACCA TCAAAAGATG AAGTTAGTCC TGGGGATGGG GGGTGGAGTT CACAGTAACC 1380 TGCACCCCCA TATCATCCAT ACTAGTCTCC TCAAAAATTC TAAAATGTGC TGGCATTTTC 1440 TCCGTGAGAT AGGAGAGACC ATATCCCCGT CCCAGAAAGC AATCACTCTC TTGGCCCCCC 1500 TTCTCAAAAG GAGCACGCTC TGTGGTGTCA CTTGTAACGT TCCAGCCAAT TTCTTACGGC 1560 ATAAACTGAC GATCTTCCAC TTGAGCAACA GAAGAGCGAG GAGCTTCCAT GAGGAGTTAT 1620 GTGCTGTCCT CGGCATGAGC CTGACCAACA GTGGGCCCTG AGTCATTAAC TACACTTGGT 1680 AACACACTGT CACTCACTGC TAAATTAACC ATTACTTTTA TATGAACACA 1730
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