| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63727999-63728157 | Common:1; Rare:74 | ||||
| chr14:63852816-63853123 | Common:1; Rare:108; Clinvar:4; Clinvar (benign):2 | ||||
| chr14:64196843-64197081 | Common:1; Rare:65 | ||||
| chr14:64209248-64209566 | Common:1; Rare:83; Clinvar:3 | ||||
| chr14:64209656-64210122 | Rare:137; Clinvar:6 | ||||
| chr14:64214030-64214358 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:64215798-64216068 | Common:1; Rare:45 | ||||
| chr14:64338051-64338155 | Common:1; Rare:22 | ||||
| chr14:64338160-64338274 | Rare:27 | ||||
| chr14:64387922-64388401 | Common:2; Rare:160 | ||||
| chr14:64503607-64503916 | Common:3; Rare:121 | ||||
| chr14:64504553-64504853 | Rare:89 | ||||
| chr14:64505227-64505381 | Rare:39 | ||||
| chr14:64540346-64540797 | Common:2; Rare:117 | ||||
| chr14:64549865-64550056 | Common:2; Rare:67 |