Tag | Content |
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EnhancerAtlas ID | HS047-17159 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:18640080-18641110 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr19:18640176-18640191 | AGAGGTCAGAGGTTG | + | 6.24 |
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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 | AAATAATAAA AAAAATTGGC CAGGTGTGGT GGCGTGCACC TGTAATCCCA GCTACTTGGG 60 AAGCTGAGGC AGGAGAATCG CTTGAACCCG GGAGGCAGAG GTCAGAGGTT GCAGTGAGCT 120 GAGATCATGC CACTGCACTC CAGCCTGGGT GACAGAGCTG GCATGCAAAA AAAAAAAAAA 180 AAAATTAGCT GGGTGTGGTG GCACATGCCT GTAATCCCAG CTACTTGGGA GGTTGAGGCA 240 GGAGAATTGC CTGAACCTGG GGCTAACCAC TGGAAAGAGA GCACAGCCTC AAGCCACACT 300 CAGCCTCAAG TCATCCAGGT GACCCAGAGA ACAAGGGCCT GGAAGAAGCG GGTGAGTGGG 360 TGAGGTGGAG GTGTAGATTG GAGTCCTAGG CCTTTGGGAG GCCCTCCAAC CTCCCTTCTG 420 CACCAACTTC TCCTGGGTGG CTGTGGCAGG CAGCTTTCCC TCCTGGGCTG TAAGGGGATA 480 GATGCAGGTG AGGTGACTGT AGTGGTCTAT TTTCAAGGAT GCCCTTATTC TTGGGGGCAA 540 GATGGAACAG CAGGAAGAAA GGGTGTGGGT GCTGGGCTGA CAGAGGCCCC GATGCTGGCT 600 CCGCCCATCC TGGCTGCACT GGTGAGCGGC ATCATAGGAG AAGCTCCCAG AGTCCAGAGT 660 TGGGAGAGCC AGATGGGATC AGGGAACCTC CCAGCATCAA CCCTGGCCCT TCCTCATGGC 720 CCCTAAAGCC CTGCAGGGTA TGGCTCTGCA GGCTACCCAG CCTCATCCAT CTGGAATGCA 780 CCAGGCTAGA CCTGGCCCCA GGGTCTTTGT ACTGGGCGTG CTGTTGCCCA GACCTGGGGC 840 TGTCGGCTTC CTGCATGGGC AGACCCTTGC CATCGCTGAA ATATCAGCGC ACACATCCCC 900 TGGGAGAGGT CTTCCTGGGC CTCCAGCTGT GCCTTCTCAC AGGCTGCATC CAGACATTCA 960 CATCCTCTCC CCTGGACCCC ATCTGTCTCT TGTTTTGAGA TGAAGTCTCC CTGTGTTGCC 1020 CAGGCTGCAG 1030
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