| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35826724-35826926 | Common:1; Rare:53 | ||||
| chr14:36320577-36320766 | Common:3; Rare:62 | ||||
| chr14:36657528-36657698 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:37172004-37172137 | Rare:37 | ||||
| chr14:37172359-37172560 | Common:2; Rare:86 | ||||
| chr14:37595391-37595634 | Common:1; Rare:66 | ||||
| chr14:39103090-39103489 | Common:3; Rare:98 | ||||
| chr14:39114103-39114346 | Common:2; Rare:74 | ||||
| chr14:39170192-39170629 | Common:4; Rare:123 | ||||
| chr14:39175165-39175301 | Common:2; Rare:62 | ||||
| chr14:39267061-39267433 | Common:2; Rare:134 | ||||
| chr14:39432407-39432653 | Common:6; Rare:85 | ||||
| chr14:44961892-44962272 | Common:3; Rare:110 | ||||
| chr14:45253078-45253312 | Rare:62 | ||||
| chr14:45253496-45253624 | Common:2; Rare:56 |