Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:420438-420547 | Common:3; Rare:21 | ||||
chr20:420896-421288 | Common:3; Rare:125; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr20:505113-505319 | Rare:31 | ||||
chr20:1161594-1161852 | Common:3; Rare:37 | ||||
chr20:1370692-1370929 | Common:1; Rare:34 | ||||
chr20:1383405-1383491 | Rare:15 | ||||
chr20:1387485-1387681 | Rare:32 | ||||
chr20:1861837-1861933 | Rare:20 | ||||
chr20:2463913-2464056 | Common:1; Rare:35 | ||||
chr20:2837223-2837435 | Rare:41 | ||||
chr20:2960695-2960833 | Common:1; Rare:23 | ||||
chr20:3021951-3022178 | Rare:47 | ||||
chr20:3784370-3784638 | Rare:53 | ||||
chr20:3785054-3785327 | Common:2; Rare:109 | ||||
chr20:3785428-3785557 | Rare:34 |