| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39114154-39114356 | Common:2; Rare:73 | ||||
| chr14:39170290-39170454 | Common:2; Rare:47 | ||||
| chr14:39175002-39175374 | Common:4; Rare:134 | ||||
| chr14:39267026-39267454 | Common:2; Rare:154 | ||||
| chr14:39432463-39432618 | Common:6; Rare:52 | ||||
| chr14:44961892-44962258 | Common:3; Rare:106 | ||||
| chr14:45083979-45084191 | Common:1; Rare:77 | ||||
| chr14:45253047-45253473 | Common:1; Rare:123 | ||||
| chr14:49586322-49586692 | Common:1; Rare:191; Clinvar (benign):1 | ||||
| chr14:49598648-49598714 | Rare:31 | ||||
| chr14:49598879-49599062 | Common:1; Rare:64 | ||||
| chr14:49620573-49620812 | Common:2; Rare:95 | ||||
| chr14:49688201-49688266 | Rare:22 | ||||
| chr14:49767998-49768264 | Common:2; Rare:99 | ||||
| chr14:49892887-49893118 | Rare:96 |