| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49621965-49622258 | Rare:83; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr14:49622406-49622875 | Rare:110; Clinvar (benign):2 | ||||
| chr14:49633585-49633669 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:49633932-49634052 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr14:49634266-49634477 | Common:1; Rare:101; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49799460-49799660 | Rare:63 | ||||
| chr14:50003757-50003941 | Common:3; Rare:50 | ||||
| chr14:50007124-50007206 | Rare:12 | ||||
| chr14:50009070-50009214 | Rare:24 | ||||
| chr14:50039852-50039994 | Common:2; Rare:31 | ||||
| chr14:50479220-50479553 | Common:3; Rare:63 | ||||
| chr14:50908049-50908118 | Common:1; Rare:10 | ||||
| chr14:50922381-50922845 | Common:3; Rare:90 | ||||
| chr14:51249469-51249768 | Common:4; Rare:90 | ||||
| chr14:51363344-51363619 | Rare:55 |