| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:36662381-36662580 | Common:2; Rare:37 | ||||
| chr14:36662755-36662844 | Common:4; Rare:16 | ||||
| chr14:36662980-36663318 | Rare:92; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr14:36760071-36760116 | Rare:7 | ||||
| chr14:36760145-36760544 | Common:4; Rare:75 | ||||
| chr14:37171707-37171925 | Rare:37 | ||||
| chr14:37172005-37172625 | Common:3; Rare:227 | ||||
| chr14:37172634-37172745 | Common:2; Rare:37 | ||||
| chr14:37197528-37197596 | Rare:10 | ||||
| chr14:37197763-37198096 | Common:3; Rare:115 | ||||
| chr14:37594587-37594688 | Common:1; Rare:16 | ||||
| chr14:37594893-37595126 | Common:1; Rare:67 | ||||
| chr14:37595158-37595284 | Rare:40 | ||||
| chr14:37595420-37595639 | Common:1; Rare:57 | ||||
| chr14:39103049-39103251 | Common:2; Rare:56 |