| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35292110-35292488 | Common:6; Rare:124; Clinvar:1 | ||||
| chr14:35292618-35292669 | Rare:16 | ||||
| chr14:35404022-35404063 | Rare:11 | ||||
| chr14:35404073-35404474 | Common:4; Rare:138; Clinvar (benign):1 | ||||
| chr14:35404582-35404900 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:35405059-35405278 | Common:1; Rare:44 | ||||
| chr14:35808642-35808848 | Rare:53 | ||||
| chr14:35808886-35808992 | Rare:21 | ||||
| chr14:35809150-35809407 | Common:1; Rare:66 | ||||
| chr14:35826028-35826510 | Common:1; Rare:120 | ||||
| chr14:35826629-35826848 | Common:1; Rare:72 | ||||
| chr14:36320053-36320245 | Rare:30 | ||||
| chr14:36320297-36320404 | Rare:19 | ||||
| chr14:36320544-36320848 | Common:5; Rare:99 | ||||
| chr14:36662076-36662280 | Common:2; Rare:71 |