Tag | Content |
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EnhancerAtlas ID | HS116-28850 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr6:6317870-6318760 |
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) |
Nr2f6(var.2) | MA0728.1 | chr6:6318535-6318550 | GAGGTTACAAGGTCA | + | 6.38 | ZNF263 | MA0528.1 | chr6:6318334-6318355 | GATGGAGGAGGGAGGAGGGAG | + | 6.72 | ZNF263 | MA0528.1 | chr6:6318341-6318362 | GAGGGAGGAGGGAGAAGGAAG | + | 7.11 | ZNF263 | MA0528.1 | chr6:6318344-6318365 | GGAGGAGGGAGAAGGAAGGAG | + | 7.24 | ZNF263 | MA0528.1 | chr6:6318337-6318358 | GGAGGAGGGAGGAGGGAGAAG | + | 7.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I006318 | chr6 | 6318234 | 6318833 |
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Enhancer Sequence | TTGGTCTCCT TCTAATGAGG GGAATCGACC ACACAGCTCC AGCATGACCA TGCTCACCTA 60 TCCCAGCAAA TAGGTGTTTA TCCCCAGTGA AACCCAGCAC AGAACACCCT TAGGAGTAAA 120 ATTAGATTTT GGTGCATGAA TGTTATTGAC AAAAAAGACT CCCTGCTCAA TGCCACTCGG 180 GGACATGAGT CTGAATGTCC CTGCCATGGC CCAGGGGAAT GATGTCTGTA TCACCAAACC 240 AGTGCTGGCA CCTGGACCTT GTCACCACTG ACAGGGCTGA GAGGAGGTCA GCTGCCGGCT 300 GCTGTACCCG GAACAGGTTT CTAGGGATCA GGCAGAGGCA AGAGGCTGGG GAAGCAGCTT 360 GCCTTGCCAG CTCACCAGGC TGCTCTGGAG AGAAATAGAG GGCTTCTATC TCTATTACTG 420 TCAGAGTCTG GCACTTCTCC CCGGCTCTGA AATTCACAGC AATGGATGGA GGAGGGAGGA 480 GGGAGAAGGA AGGAGGTGCA AGCCAGACAA TCAAAACAGC CACAATATTT TGGAAGTGGA 540 ATATTCCAGC TAGAGAAAAT TCTCTAAAGC ATTGAGCAGT AGGGCTGGAA GAGGCCCTAG 600 CTAATCCAGC ACTCTGGTTT TGTAGAGGAA ATAGTTGAGA GGCAGAAAGA CAAAGCAACT 660 TCTCTGAGGT TACAAGGTCA GTAAGGGGCA GAACTGGGAC AAGGCTCTGG GTCTTCGGTG 720 CTTTCACCAC TTAAAAGAAA GCTTTTGCTT TCTTCCTTTA TAAAACCAGA GATTGGCAGG 780 GGGCTTCCTT TTGTGGGAAC CCCAGTGGAG ACAGAGGATG TTTACCTGCA GGGAAGAGGG 840 GCCAGGGCCC GGCTGTGCCT GGACCCAGAG TGGTGGGGAA GGGGGGTATG 890
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