Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110225882-110226185 | Common:1; Rare:82 | ||||
chr10:110304875-110305054 | Common:2; Rare:64 | ||||
chr10:110567381-110567805 | Common:2; Rare:130; Clinvar:2; Clinvar (benign):5 | ||||
chr10:110871745-110872016 | Rare:89 | ||||
chr10:110919294-110919654 | Common:7; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
chr10:112183708-112183844 | Common:2; Rare:52 | ||||
chr10:112376141-112376312 | Rare:32 | ||||
chr10:112446742-112447346 | Common:3; Rare:147 | ||||
chr10:112950138-112950371 | Common:3; Rare:44 | ||||
chr10:112950410-112950787 | Common:4; Rare:69 | ||||
chr10:113854352-113854885 | Common:1; Rare:121 | ||||
chr10:113855013-113855057 | Rare:15 | ||||
chr10:114304905-114305041 | Rare:37 | ||||
chr10:114404446-114404618 | Common:1; Rare:54 | ||||
chr10:114684382-114684618 | Common:2; Rare:37 |