Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42938364-42938402 | Rare:3 | ||||
chr1:42949398-42949668 | Common:1; Rare:31 | ||||
chr1:43120498-43120533 | Rare:10 | ||||
chr1:43199064-43199399 | Common:1; Rare:57 | ||||
chr1:43221327-43221434 | Rare:22 | ||||
chr1:43239576-43239770 | Rare:33 | ||||
chr1:43348959-43349266 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
chr1:43349393-43349634 | Rare:53 | ||||
chr1:43358158-43358246 | Rare:16 | ||||
chr1:43454509-43454785 | Rare:63 | ||||
chr1:43835176-43835226 | Rare:9 | ||||
chr1:44030040-44030148 | Rare:47 | ||||
chr1:44030273-44030464 | Rare:71 | ||||
chr1:44068737-44068866 | Common:1; Rare:17 | ||||
chr1:44676529-44676702 | Common:2; Rare:25 |