Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:36050428-36050732 | Common:1; Rare:113 | ||||
chr20:40619786-40619952 | Common:2; Rare:38 | ||||
chr20:40687129-40687143 | |||||
chr20:40687718-40687734 | Rare:4; Clinvar (benign):2 | ||||
chr20:41030641-41030723 | Rare:13 | ||||
chr20:45344539-45344767 | Common:2; Rare:42 | ||||
chr20:45899460-45899667 | Rare:72 | ||||
chr20:47357794-47357856 | Rare:13 | ||||
chr20:48025107-48025238 | Common:1; Rare:25 | ||||
chr20:50192106-50192448 | Common:2; Rare:89 | ||||
chr20:50321389-50321595 | Rare:42 | ||||
chr20:50415692-50415927 | Common:1; Rare:69 | ||||
chr20:62306611-62306670 | Rare:23 | ||||
chr20:62307130-62307439 | Common:1; Rare:95 | ||||
chr20:62624011-62624180 | Common:1; Rare:39 |