Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73569005-73569294 | Rare:66 | ||||
chr14:73644891-73645031 | Common:2; Rare:41; Clinvar:2 | ||||
chr14:73714376-73714462 | Common:1; Rare:33 | ||||
chr14:73787123-73787365 | Common:2; Rare:85 | ||||
chr14:73851723-73851983 | Common:4; Rare:85 | ||||
chr14:73950167-73950333 | Common:3; Rare:74; Clinvar (benign):1 | ||||
chr14:74019184-74019428 | Common:2; Rare:94 | ||||
chr14:74084396-74084597 | Common:2; Rare:57 | ||||
chr14:74302899-74303045 | Common:1; Rare:74; Clinvar (benign):3 | ||||
chr14:74493232-74493781 | Common:4; Rare:176; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713052-74713209 | Rare:88 | ||||
chr14:74763127-74763397 | Rare:83 | ||||
chr14:74881821-74881973 | Rare:69 | ||||
chr14:75002741-75002982 | Common:1; Rare:79; Clinvar:2 | ||||
chr14:75069270-75069680 | Common:2; Rare:108 |