| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73644825-73645049 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73714358-73714504 | Common:1; Rare:52 | ||||
| chr14:73787121-73787379 | Common:2; Rare:88 | ||||
| chr14:73851759-73851974 | Common:4; Rare:75 | ||||
| chr14:73886785-73886869 | Common:1; Rare:25 | ||||
| chr14:73950050-73950333 | Common:6; Rare:122; Clinvar (benign):5 | ||||
| chr14:74019221-74019455 | Common:2; Rare:86 | ||||
| chr14:74302915-74303060 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr14:74493261-74493777 | Common:4; Rare:164; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713058-74713203 | Rare:79 | ||||
| chr14:75002746-75002967 | Common:1; Rare:65; Clinvar:2 | ||||
| chr14:75063977-75064179 | Common:1; Rare:50 | ||||
| chr14:75126960-75127110 | Rare:53 | ||||
| chr14:75176509-75176710 | Rare:66 | ||||
| chr14:75278739-75279001 | Common:3; Rare:68 |