| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73239439-73239616 | Common:1; Rare:38 | ||||
| chr14:73458513-73458857 | Common:5; Rare:90 | ||||
| chr14:73569258-73569292 | Rare:11 | ||||
| chr14:73644885-73645030 | Common:2; Rare:41; Clinvar:2 | ||||
| chr14:73787166-73787350 | Common:2; Rare:72 | ||||
| chr14:73790090-73790391 | Common:2; Rare:49 | ||||
| chr14:73950153-73950330 | Common:3; Rare:79; Clinvar (benign):1 | ||||
| chr14:74019241-74019452 | Common:1; Rare:78 | ||||
| chr14:74493240-74493781 | Common:4; Rare:172; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713057-74713200 | Rare:79 | ||||
| chr14:74881833-74881975 | Rare:66 | ||||
| chr14:75002746-75002967 | Common:1; Rare:65; Clinvar:2 | ||||
| chr14:75069478-75069689 | Common:1; Rare:52 | ||||
| chr14:75126989-75127110 | Rare:39 | ||||
| chr14:75278376-75278546 | Rare:34 |