| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73887255-73887428 | Common:1; Rare:32 | ||||
| chr14:73949822-73949982 | Common:4; Rare:51 | ||||
| chr14:73950043-73950461 | Common:6; Rare:175; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:73950494-73950614 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr14:74018582-74019486 | Common:8; Rare:240 | ||||
| chr14:74084171-74084263 | Common:1; Rare:16 | ||||
| chr14:74084338-74084619 | Common:2; Rare:84 | ||||
| chr14:74085193-74085520 | Common:4; Rare:47 | ||||
| chr14:74085543-74085583 | Rare:7 | ||||
| chr14:74085585-74085792 | Common:2; Rare:28 | ||||
| chr14:74302669-74302700 | Rare:8 | ||||
| chr14:74302859-74303159 | Common:3; Rare:121; Clinvar (benign):3 | ||||
| chr14:74492901-74493081 | Rare:20 | ||||
| chr14:74493179-74493834 | Common:4; Rare:223; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74494097-74494221 | Rare:53; Clinvar (benign):1 |