| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35404627-35404858 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:36320580-36320764 | Common:3; Rare:59 | ||||
| chr14:37197865-37198082 | Common:3; Rare:69 | ||||
| chr14:37595395-37595639 | Common:1; Rare:66 | ||||
| chr14:39103591-39103727 | Common:2; Rare:29 | ||||
| chr14:39174705-39174973 | Common:3; Rare:71 | ||||
| chr14:39267081-39267396 | Common:1; Rare:104 | ||||
| chr14:39432418-39432657 | Common:6; Rare:81 | ||||
| chr14:44961886-44962259 | Common:3; Rare:109 | ||||
| chr14:45253088-45253323 | Rare:66 | ||||
| chr14:49586337-49586776 | Common:1; Rare:236 | ||||
| chr14:49598648-49599031 | Common:2; Rare:146 | ||||
| chr14:49620563-49620837 | Common:2; Rare:114; Clinvar:3 | ||||
| chr14:49688193-49688287 | Rare:37 | ||||
| chr14:49768016-49768283 | Common:2; Rare:99 |