| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:58427523-58427749 | Rare:78 | ||||
| chr14:59188427-59188774 | Common:2; Rare:91 | ||||
| chr14:59484026-59484182 | Common:1; Rare:73 | ||||
| chr14:59484312-59484569 | Common:3; Rare:103 | ||||
| chr14:60091824-60092233 | Common:5; Rare:145 | ||||
| chr14:60724306-60724520 | Common:1; Rare:52 | ||||
| chr14:60980982-60981264 | Rare:111 | ||||
| chr14:61321456-61321751 | Common:3; Rare:80 | ||||
| chr14:61322816-61322967 | Rare:22 | ||||
| chr14:61762218-61762447 | Common:2; Rare:71 | ||||
| chr14:63543342-63543609 | Common:3; Rare:72 | ||||
| chr14:63641823-63642089 | Common:3; Rare:87 | ||||
| chr14:63728007-63728135 | Common:1; Rare:60 | ||||
| chr14:63852874-63853061 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:64388154-64388404 | Common:2; Rare:119 |