Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73760248-73760410 | Common:1; Rare:37 | ||||
chr14:73886813-73886893 | Common:1; Rare:25 | ||||
chr14:73950041-73950467 | Common:6; Rare:176; Clinvar:1; Clinvar (benign):5 | ||||
chr14:74019256-74019467 | Common:1; Rare:80 | ||||
chr14:74084392-74084780 | Common:7; Rare:99 | ||||
chr14:74493290-74493781 | Common:4; Rare:154; Clinvar:2; Clinvar (benign):4 | ||||
chr14:74713017-74713207 | Common:1; Rare:107 | ||||
chr14:74763058-74763448 | Rare:108 | ||||
chr14:74763687-74764020 | Rare:120 | ||||
chr14:74809966-74810240 | Rare:51 | ||||
chr14:74881810-74881990 | Rare:83 | ||||
chr14:74923188-74923494 | Common:5; Rare:73 | ||||
chr14:75002741-75002972 | Common:1; Rare:72; Clinvar:2 | ||||
chr14:75051418-75051530 | Common:2; Rare:32; Clinvar:3; Clinvar (benign):2 | ||||
chr14:75063953-75064179 | Common:1; Rare:59 |