Tag | Content |
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EnhancerAtlas ID | HS076-13854 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr12:57069390-57070030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:57069488-57069503 | AAGGTCAGGAGTTCA | + | 6.04 | ZNF263 | MA0528.1 | chr12:57069926-57069947 | GGGGGAGGTGGAGGTGGAGGT | + | 6.21 | ZNF263 | MA0528.1 | chr12:57069917-57069938 | GGAGGGGGAGGGGGAGGTGGA | + | 6.32 | ZNF263 | MA0528.1 | chr12:57069911-57069932 | GGAGGGGGAGGGGGAGGGGGA | + | 7.23 | ZNF263 | MA0528.1 | chr12:57069920-57069941 | GGGGGAGGGGGAGGTGGAGGT | + | 7.34 | ZNF263 | MA0528.1 | chr12:57069914-57069935 | GGGGGAGGGGGAGGGGGAGGT | + | 8.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGTTGGCTA ACACATTAAA ACTACAAACA GGGCCGAGTG CGGTGGCTCA CGCCTGTAAT 60 CTCCAGCACT TTGGGAGGCT GAGATGGGTG CATCACCTAA GGTCAGGAGT TCAGAGACCA 120 GCCTGGCAAA CATTATGAAA CCCCATCTCT ACTAAAAATA CAAAAAATTA GCTGGGTGTG 180 GTGATGGGCA CCTGTAATCC CAGCTACTCA GGATGCTGCA GCAGGAGAAT CGCTTGAAAT 240 AAGGAGGTGG AGGTTGCAGT GAGCCCAGAC CACGCCATTG CACTCCAGCC TGGACAACAG 300 CGTGAAACTC CGTCTCAAAA CACAACACAA AAACTGCAGA CCAGGCGCAG TGACTCAAGC 360 CCATGATCCC AGCACTTTGT GAGGCCAAGG CTGATGGATC ACCTGGGGCT GGGAGTTTGA 420 GACCAGTCTG ACCAACGTGG AGAAACCCCG TCTCTACTAA AAATACAAAA TTAGCCAGGC 480 GAGGTGGCGT ATGCCTGTAA TACCAGCTAT TTGGGAGGCT GGGAGGGGGA GGGGGAGGGG 540 GAGGTGGAGG TGGAGGTTGC GGTAAGCCGA GATCACGCCA CTGCACTACA GCCTGGGCAA 600 CAGAGAGAGG CTGTGTCTCC CCCCCCAAAA AAAAAAAAAA 640
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