Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73851592-73852009 | Common:5; Rare:118 | ||||
chr14:73950071-73950348 | Common:6; Rare:124; Clinvar (benign):4 | ||||
chr14:73996059-73996344 | Common:1; Rare:62 | ||||
chr14:74019233-74019436 | Common:1; Rare:81 | ||||
chr14:74493234-74493791 | Common:4; Rare:182; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713068-74713200 | Rare:71 | ||||
chr14:74763165-74763435 | Rare:83 | ||||
chr14:74881831-74881973 | Rare:65 | ||||
chr14:75002726-75003035 | Common:1; Rare:107; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr14:75063581-75063728 | Common:1; Rare:30 | ||||
chr14:75063988-75064192 | Common:1; Rare:51 | ||||
chr14:75069301-75069732 | Common:2; Rare:108 | ||||
chr14:75126969-75127110 | Rare:50 | ||||
chr14:75147670-75147910 | Common:3; Rare:45 | ||||
chr14:75176440-75176854 | Common:1; Rare:112 |