Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73058303-73058632 | Common:3; Rare:101 | ||||
chr14:73569022-73569286 | Rare:58 | ||||
chr14:73787121-73787379 | Common:2; Rare:88 | ||||
chr14:73851724-73851983 | Common:4; Rare:85 | ||||
chr14:73886785-73886897 | Common:2; Rare:38 | ||||
chr14:73950050-73950330 | Common:6; Rare:120; Clinvar (benign):5 | ||||
chr14:74019237-74019484 | Common:1; Rare:91 | ||||
chr14:74084628-74084989 | Common:7; Rare:112 | ||||
chr14:74302922-74303040 | Common:1; Rare:58; Clinvar (benign):1 | ||||
chr14:74493376-74493781 | Common:4; Rare:123; Clinvar (benign):4 | ||||
chr14:74713042-74713223 | Rare:101 | ||||
chr14:74881781-74881964 | Common:1; Rare:81 | ||||
chr14:75002741-75002952 | Common:1; Rare:60; Clinvar:2 | ||||
chr14:75063988-75064179 | Common:1; Rare:48 | ||||
chr14:75069340-75069732 | Common:2; Rare:95 |