Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40059267-40059466 | Common:1; Rare:47 | ||||
chr1:40064933-40065023 | Rare:12 | ||||
chr1:40186545-40186779 | Common:1; Rare:45 | ||||
chr1:40232607-40232641 | Rare:6 | ||||
chr1:40312531-40312744 | Common:1; Rare:62; Clinvar (benign):5 | ||||
chr1:40381544-40381737 | Rare:35 | ||||
chr1:40383611-40383720 | Rare:13 | ||||
chr1:40384348-40384603 | Rare:35 | ||||
chr1:40386087-40386216 | Rare:18 | ||||
chr1:40394956-40395017 | Common:1; Rare:8 | ||||
chr1:40628386-40628801 | Common:1; Rare:70 | ||||
chr1:40699865-40700002 | Common:1; Rare:30 | ||||
chr1:40702926-40703178 | Rare:56 | ||||
chr1:40711932-40711949 | Rare:1 | ||||
chr1:40809636-40809683 | Common:1; Rare:11 |