Tag | Content |
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EnhancerAtlas ID | HS091-00444 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:12090550-12091320 |
Target genes | Number: 17 | Name | Ensembl ID |
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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) |
ZNF263 | MA0528.1 | chr1:12090934-12090955 | GGAGGAGAAGGATGCAGAGGA | + | 6.59 |
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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 | GGGGGAGGCG CCTTGGTGGA GGAGCTGGGA TTCGAACCTA GGTCTCTGTG CTGCTGCTGC 60 TGCTTTTTTT TTTTTTTTTT TTTTTTGAGA CCGAGTTTTG TTCTTACTGC CCAGGCTGGA 120 GTGCATTGGC ATGGTCTCAG CTCACTGCAG CCTCCACTGT AGTCCCAGCT ACTTGGGAGG 180 CTGAGGTGGG AGGATCGCTT GAACCTGGGA GGCAGAGGCT GCAGTGAGCT GAGATCTCGC 240 CACTGCACTG CAGCCTGGGT GACAGAGTGA GACTCCATCT CAAAAAAAAA AAAAATGTCC 300 TTTCCTGTGT CTCCAGGTCG GGATGGGGTG CCAGTGGCAA CTCCCCCTGA CTCCTAAATT 360 GAGAGTAGGG CAGCTGGGGT CAGAGGAGGA GAAGGATGCA GAGGAAAGTC AGTTTGCTGG 420 TCCGTAAAAT GGACATAACA GCGCCATCCT CAGGGATGTT GGTGGTGAGG TGGGGCTGTT 480 GAGTGAAGCA ATCCATGCAG GTGCTTGGAG AGCCTACAGC AGGAAGTACC CTGTGAATGT 540 CACTGTCACC GTCCTATCCT CCTCCCATTT CAGCTCTCAG GGCCCCAGGG ATGGCTGGAT 600 CTGCCAGGAT AAGAAAGGGG AGAGCTGGGG TAGTCTTGTG GGTAGACACA GGCCCTGCCT 660 TGGTGGGGGC CTCCTTCCTA ATGGGGGGCA CAGTTCCTCC CTGATGGGGG TGTGCCCAGT 720 CAGCGGGGAG CTTGTCCCAG GTCAGGCACT TTTAACTCCT TGCCTTCCAC 770
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