| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39432915-39433015 | Rare:30 | ||||
| chr14:44961896-44962266 | Common:3; Rare:108 | ||||
| chr14:45253078-45253299 | Rare:58 | ||||
| chr14:45253442-45253573 | Common:2; Rare:54 | ||||
| chr14:49586327-49586776 | Common:1; Rare:240; Clinvar (benign):1 | ||||
| chr14:49598667-49599014 | Common:2; Rare:133 | ||||
| chr14:49620561-49620830 | Common:2; Rare:110; Clinvar:3 | ||||
| chr14:49767587-49767706 | Common:2; Rare:40 | ||||
| chr14:49892895-49893126 | Rare:98 | ||||
| chr14:50116556-50116709 | Common:1; Rare:67 | ||||
| chr14:50312143-50312380 | Rare:107; Clinvar (benign):1 | ||||
| chr14:50396870-50396991 | Common:1; Rare:32 | ||||
| chr14:50532481-50532624 | Common:2; Rare:43 | ||||
| chr14:50561080-50561196 | Rare:22 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 |