| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39175630-39176270 | Common:9; Rare:194 | ||||
| chr14:39178860-39179450 | Common:1; Rare:252 | ||||
| chr14:39233803-39234017 | Rare:67 | ||||
| chr14:39266569-39266711 | Common:4; Rare:84 | ||||
| chr14:39267032-39267492 | Common:6; Rare:312 | ||||
| chr14:39432389-39432674 | Common:13; Rare:190 | ||||
| chr14:39432770-39433080 | Rare:130 | ||||
| chr14:44897003-44897346 | Common:2; Rare:212 | ||||
| chr14:44961892-44962259 | Common:6; Rare:209 | ||||
| chr14:45083938-45084166 | Common:1; Rare:91 | ||||
| chr14:45253061-45253299 | Rare:105 | ||||
| chr14:45253450-45253710 | Common:3; Rare:165 | ||||
| chr14:49586294-49586605 | Common:2; Rare:237; Clinvar (benign):1 | ||||
| chr14:49598631-49599025 | Common:5; Rare:290 | ||||
| chr14:49620570-49620855 | Common:4; Rare:226; Clinvar:7 |