| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:46100941-46101097 | Common:3; Rare:48 | ||||
| chr14:46402041-46403138 | Common:13; Rare:488 | ||||
| chr14:46820260-46820640 | Common:4; Rare:134 | ||||
| chr14:47675602-47675747 | Common:1; Rare:37 | ||||
| chr14:47676043-47676160 | Rare:46 | ||||
| chr14:48325726-48326126 | Rare:152 | ||||
| chr14:48561330-48561890 | Common:5; Rare:114 | ||||
| chr14:48952620-48953085 | Common:6; Rare:206 | ||||
| chr14:49527960-49528503 | Rare:163 | ||||
| chr14:49633741-49634145 | Common:7; Rare:361; Clinvar:36; Clinvar (benign):17; Clinvar (pathogenic):5 | ||||
| chr14:49634173-49634630 | Common:3; Rare:567; Clinvar:38; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr14:49644699-49645185 | Common:8; Rare:155 | ||||
| chr14:49775890-49776526 | Common:5; Rare:168 | ||||
| chr14:49851576-49852110 | Common:2; Rare:204 | ||||
| chr14:49861643-49862043 | Common:1; Rare:156 |