| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73058347-73058622 | Common:3; Rare:87 | ||||
| chr14:73458503-73458857 | Common:5; Rare:93 | ||||
| chr14:73569031-73569302 | Rare:59 | ||||
| chr14:73644901-73645037 | Common:2; Rare:36; Clinvar:2 | ||||
| chr14:73714360-73714440 | Common:1; Rare:31 | ||||
| chr14:73787125-73787379 | Common:2; Rare:88 | ||||
| chr14:73851733-73851983 | Common:4; Rare:85 | ||||
| chr14:73886785-73886925 | Common:2; Rare:43 | ||||
| chr14:73950033-73950333 | Common:6; Rare:126; Clinvar (benign):5 | ||||
| chr14:74019254-74019436 | Common:1; Rare:72 | ||||
| chr14:74084658-74084987 | Common:5; Rare:106 | ||||
| chr14:74302910-74303134 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chr14:74493240-74493789 | Common:4; Rare:177; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713052-74713213 | Rare:90 | ||||
| chr14:74763136-74763430 | Rare:89 |