| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73851596-73852013 | Common:6; Rare:117 | ||||
| chr14:73858430-73858686 | Common:2; Rare:49 | ||||
| chr14:73950130-73950333 | Common:4; Rare:87; Clinvar (benign):2 | ||||
| chr14:74019221-74019511 | Common:2; Rare:108 | ||||
| chr14:74084395-74084661 | Common:4; Rare:67 | ||||
| chr14:74493227-74493781 | Common:4; Rare:178; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713058-74713257 | Rare:102 | ||||
| chr14:74763159-74763408 | Rare:78 | ||||
| chr14:75051418-75051527 | Common:2; Rare:31; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75069377-75069680 | Common:2; Rare:73 | ||||
| chr14:75126954-75127128 | Rare:63 | ||||
| chr14:75279057-75279123 | Rare:19 | ||||
| chr14:75279379-75279660 | Common:1; Rare:56 | ||||
| chr14:75280371-75280777 | Common:3; Rare:100 | ||||
| chr14:75427903-75428239 | Rare:79 |