| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45253067-45253325 | Rare:74 | ||||
| chr14:49586359-49586617 | Common:1; Rare:113 | ||||
| chr14:49598666-49599029 | Common:2; Rare:137 | ||||
| chr14:49620570-49620859 | Common:2; Rare:116; Clinvar:4 | ||||
| chr14:49635179-49635336 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr14:49688121-49688380 | Common:2; Rare:99 | ||||
| chr14:49692800-49693190 | Common:1; Rare:110 | ||||
| chr14:49767554-49767723 | Common:2; Rare:65 | ||||
| chr14:49767930-49768162 | Common:2; Rare:77 | ||||
| chr14:49768384-49768784 | Rare:144 | ||||
| chr14:49852741-49853189 | Common:4; Rare:119 | ||||
| chr14:49892857-49893130 | Rare:125 | ||||
| chr14:50116507-50116758 | Common:1; Rare:130 | ||||
| chr14:50231059-50231253 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr14:50231527-50231808 | Common:1; Rare:79 |