| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73058317-73058631 | Common:3; Rare:98 | ||||
| chr14:73567468-73567653 | Common:1; Rare:44 | ||||
| chr14:73569020-73569300 | Rare:63 | ||||
| chr14:73713794-73714023 | Rare:61 | ||||
| chr14:73787121-73787372 | Common:2; Rare:87 | ||||
| chr14:73790065-73790314 | Common:1; Rare:40 | ||||
| chr14:73851592-73851983 | Common:4; Rare:112 | ||||
| chr14:73950062-73950333 | Common:6; Rare:117; Clinvar (benign):4 | ||||
| chr14:74019248-74019455 | Common:1; Rare:76 | ||||
| chr14:74302915-74303056 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr14:74493229-74493795 | Common:4; Rare:186; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74611562-74611598 | Rare:11 | ||||
| chr14:74611600-74611680 | Rare:27 | ||||
| chr14:74612583-74612863 | Common:1; Rare:72 | ||||
| chr14:74713053-74713209 | Rare:86 |