| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35122487-35122621 | Common:1; Rare:48 | ||||
| chr14:35122710-35122787 | Rare:25 | ||||
| chr14:35292193-35292495 | Common:5; Rare:109; Clinvar:1 | ||||
| chr14:35826297-35826512 | Common:1; Rare:64 | ||||
| chr14:35826692-35826929 | Common:1; Rare:69 | ||||
| chr14:39103199-39103292 | Rare:25 | ||||
| chr14:39174970-39175304 | Common:5; Rare:118 | ||||
| chr14:39179092-39179462 | Common:1; Rare:99 | ||||
| chr14:39267047-39267417 | Common:2; Rare:128 | ||||
| chr14:44961892-44962258 | Common:3; Rare:106 | ||||
| chr14:45084002-45084181 | Rare:63 | ||||
| chr14:45253078-45253282 | Rare:54 | ||||
| chr14:49598663-49599036 | Common:2; Rare:139 | ||||
| chr14:49620573-49620818 | Common:2; Rare:97; Clinvar:1 | ||||
| chr14:49621183-49621584 | Common:1; Rare:149; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |