| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39448593-39448793 | Rare:40 | ||||
| chr14:44962748-44962868 | Rare:31 | ||||
| chr14:45252115-45252210 | Rare:24 | ||||
| chr14:45252276-45252521 | Common:1; Rare:64 | ||||
| chr14:49597725-49597858 | Rare:26 | ||||
| chr14:49599731-49599791 | Common:1; Rare:15 | ||||
| chr14:49624258-49624444 | Rare:37 | ||||
| chr14:49631581-49631702 | Common:1; Rare:22 | ||||
| chr14:49633071-49633102 | Rare:8 | ||||
| chr14:49633534-49633710 | Common:1; Rare:70; Clinvar:7; Clinvar (benign):5 | ||||
| chr14:49633818-49634166 | Common:1; Rare:130; Clinvar:14; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr14:49853862-49853896 | Rare:6 | ||||
| chr14:49853914-49853989 | Rare:9 | ||||
| chr14:49861620-49861921 | Common:1; Rare:69 | ||||
| chr14:49862025-49862196 | Rare:35 |