| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74881711-74882032 | Common:3; Rare:329 | ||||
| chr14:74922340-74922760 | Common:7; Rare:179 | ||||
| chr14:74923171-74923358 | Common:1; Rare:56 | ||||
| chr14:74955549-74955738 | Common:2; Rare:62 | ||||
| chr14:75002633-75003017 | Common:3; Rare:326; Clinvar:6; Clinvar (pathogenic):3 | ||||
| chr14:75050655-75051300 | Common:2; Rare:186 | ||||
| chr14:75051344-75051564 | Common:3; Rare:101; Clinvar:5; Clinvar (benign):3 | ||||
| chr14:75063944-75064233 | Common:3; Rare:186 | ||||
| chr14:75069220-75069740 | Common:4; Rare:257 | ||||
| chr14:75126946-75127128 | Rare:94 | ||||
| chr14:75176033-75176397 | Common:2; Rare:135 | ||||
| chr14:75176474-75176663 | Rare:123 | ||||
| chr14:75176800-75177100 | Rare:118 | ||||
| chr14:75277663-75279066 | Common:17; Rare:565 | ||||
| chr14:75427320-75427760 | Rare:236 |