| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35292179-35292484 | Common:5; Rare:108; Clinvar:1 | ||||
| chr14:35404634-35404983 | Common:2; Rare:111; Clinvar (benign):2 | ||||
| chr14:35826724-35826926 | Common:1; Rare:53 | ||||
| chr14:39170261-39170483 | Common:3; Rare:67 | ||||
| chr14:39174909-39175285 | Common:5; Rare:131 | ||||
| chr14:39267335-39267422 | Rare:43 | ||||
| chr14:39432424-39432618 | Common:6; Rare:62 | ||||
| chr14:44961892-44962258 | Common:3; Rare:106 | ||||
| chr14:45135723-45135979 | Common:1; Rare:48 | ||||
| chr14:45253100-45253282 | Rare:46 | ||||
| chr14:49586320-49586719 | Common:1; Rare:206; Clinvar (benign):1 | ||||
| chr14:49598731-49599020 | Common:1; Rare:106 | ||||
| chr14:49620561-49620842 | Common:2; Rare:117; Clinvar:3 | ||||
| chr14:49688184-49688278 | Rare:37 | ||||
| chr14:49892913-49893136 | Rare:91 |