Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154936590-154937578 | Common:5; Rare:239 | ||||
chr1:154956068-154956290 | Common:1; Rare:65 | ||||
chr1:154961298-154961621 | Rare:95 | ||||
chr1:154961636-154961913 | Common:1; Rare:99 | ||||
chr1:154961976-154962165 | Rare:54 | ||||
chr1:154962446-154962489 | Common:1; Rare:15 | ||||
chr1:154962491-154962547 | Rare:18 | ||||
chr1:154970629-154970869 | Rare:40 | ||||
chr1:154973707-154973933 | Rare:63 | ||||
chr1:154974038-154974265 | Common:3; Rare:62 | ||||
chr1:154974270-154974739 | Rare:117 | ||||
chr1:154974814-154975304 | Common:3; Rare:140 | ||||
chr1:154975489-154975657 | Rare:30 | ||||
chr1:154975709-154975988 | Common:1; Rare:57 | ||||
chr1:154983062-154983440 | Common:2; Rare:80; Clinvar (benign):2 |