| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96364092-96364254 | Rare:36 | ||||
| chr14:96391687-96392167 | Common:3; Rare:134 | ||||
| chr14:96501775-96502133 | Rare:107 | ||||
| chr14:96502166-96502474 | Common:1; Rare:105 | ||||
| chr14:96502712-96502951 | Common:4; Rare:73 | ||||
| chr14:96797318-96797445 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:99480706-99481032 | Common:2; Rare:119 | ||||
| chr14:99481063-99481487 | Rare:117 | ||||
| chr14:99604167-99604489 | Common:3; Rare:98 | ||||
| chr14:99683768-99684309 | Common:2; Rare:112 | ||||
| chr14:99971256-99971428 | Common:1; Rare:59 | ||||
| chr14:100065237-100065509 | Rare:53 | ||||
| chr14:100066324-100066526 | Common:2; Rare:41 | ||||
| chr14:100238040-100238174 | Common:1; Rare:41 | ||||
| chr14:100238509-100238911 | Common:3; Rare:119 |