| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101762289-101762697 | Common:2; Rare:191 | ||||
| chr14:101763237-101764089 | Common:29; Rare:265 | ||||
| chr14:101785913-101786313 | Common:2; Rare:63 | ||||
| chr14:101809585-101810544 | Common:8; Rare:623 | ||||
| chr14:101964291-101965082 | Common:19; Rare:601; Clinvar:12; Clinvar (benign):21; Clinvar (pathogenic):2 | ||||
| chr14:102084451-102084920 | Common:1; Rare:360 | ||||
| chr14:102086179-102086602 | Common:6; Rare:350 | ||||
| chr14:102086935-102087458 | Common:30; Rare:960 | ||||
| chr14:102087400-102087890 | Common:8; Rare:352 | ||||
| chr14:102138361-102139540 | Common:6; Rare:736 | ||||
| chr14:102139460-102140018 | Common:1; Rare:809 | ||||
| chr14:102264830-102265190 | Rare:55 | ||||
| chr14:102304800-102305020 | Common:1; Rare:67 | ||||
| chr14:102305002-102305402 | Common:4; Rare:327 | ||||
| chr14:102316527-102317312 | Common:29; Rare:712 |