Tag | Content |
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EnhancerAtlas ID | HS116-22814 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr22:50697030-50697840 |
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) |
MAFG | MA0659.1 | chr22:50697222-50697243 | CAACTGCCGCCTCAGCATTTT | - | 6.15 | MITF | MA0620.2 | chr22:50697209-50697227 | ACAGGTCATGTGACAACT | + | 6.02 | MITF | MA0620.2 | chr22:50697209-50697227 | ACAGGTCATGTGACAACT | - | 6.02 | ZNF263 | MA0528.1 | chr22:50697644-50697665 | TGTGGAGGGAGGAGGAGAGGG | + | 6.39 | ZNF263 | MA0528.1 | chr22:50697648-50697669 | GAGGGAGGAGGAGAGGGAACA | + | 6.61 | ZNF263 | MA0528.1 | chr22:50697654-50697675 | GGAGGAGAGGGAACAGAGGGG | + | 6.66 |
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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 | GGGCTCCTGC CGCCTGACCC TTTCACCCCT CTTCACCCCA ACCAAACAGA TCCAGGCCCA 60 GGGTGGGGAC AGCGCTATGG AAAGAGGCCA GGCCTCTGCT GGTGAGGCCC AGGCGGACAG 120 CACCGTGACC CACCAGACCT GGTCCCCTCA GCACCCCTGG TTGGGGAGAT AGACAGTAGA 180 CAGGTCATGT GACAACTGCC GCCTCAGCAT TTTGGGGTGA CGGTCCCAGG GAGGCCTGGA 240 GTTTTGCACA GCCAAGGGTG GAGGGGCAGG TAGACATGTG GGCTGCGGGA CACCTGGCAG 300 AGGGCACACA CAGAGTGGCC GAGGCAGGAG GGAGCACACT TGGATAGTTT GAAGAATACA 360 GGGAGGGAGG CCAGGTGGCG GAGGCCCAGG CCAGGGAGGG GCTGAGGAGA GGCCAGAGGG 420 AGCCGGCAGG GCAGCACACA CCAGGTGGAA GTTTGGCTTT GATCCCAAGA GACGGGGACG 480 ATTTAAATGG GGACGTGAGG CTAAATGCGT CCTCCTGGCC GTGGTGTAGG AACCGGCCAG 540 AGTGAGGTAA GAATGGACAC AAGCTGGAAG GACAGCTCCG CCGGAGCCAC GTGGGCCAGA 600 GCCATGGGCA AGAATGTGGA GGGAGGAGGA GAGGGAACAG AGGGGGTGTC CAGGGGGCAG 660 CGGGGACTGT GGACATGAGA GCTGGAGGGT GCCCGGGAGA GTGCTTTAGC AGAAGACGGA 720 GAGCAGGGTC CTGTGGGCTA GGGGCCACAG GACTTGGCCT GGCCTCTGTG GTATGGGGGC 780 TGGCCTGGAG AGGGAGGCGG CCTGGCAGGA 810
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