| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34982504-34982690 | Common:1; Rare:77 | ||||
| chr14:35046105-35046575 | Common:2; Rare:162 | ||||
| chr14:35122239-35122781 | Common:2; Rare:156 | ||||
| chr14:35292224-35292484 | Common:4; Rare:93; Clinvar:1 | ||||
| chr14:35826734-35826926 | Common:1; Rare:50 | ||||
| chr14:36320584-36320760 | Common:3; Rare:56 | ||||
| chr14:37197813-37198103 | Common:3; Rare:97 | ||||
| chr14:39114205-39114356 | Common:2; Rare:60 | ||||
| chr14:39170237-39170424 | Common:3; Rare:50 | ||||
| chr14:39174907-39175282 | Common:5; Rare:130 | ||||
| chr14:39267026-39267406 | Common:2; Rare:123 | ||||
| chr14:44961908-44962233 | Common:2; Rare:93 | ||||
| chr14:45083944-45084174 | Common:1; Rare:92 | ||||
| chr14:45253094-45253316 | Rare:59 | ||||
| chr14:49586317-49586772 | Common:1; Rare:238; Clinvar (benign):1 |