| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74763553-74763762 | Rare:64 | ||||
| chr14:74881712-74882063 | Common:1; Rare:141 | ||||
| chr14:74882231-74882317 | Rare:23 | ||||
| chr14:74882328-74882411 | Common:2; Rare:30 | ||||
| chr14:74923207-74923368 | Common:1; Rare:48 | ||||
| chr14:74955562-74955709 | Common:1; Rare:32 | ||||
| chr14:75002526-75003129 | Common:1; Rare:187; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75051284-75051547 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75063521-75063752 | Common:1; Rare:46 | ||||
| chr14:75063947-75064188 | Common:1; Rare:62 | ||||
| chr14:75069140-75069322 | Common:3; Rare:68 | ||||
| chr14:75069539-75069703 | Common:1; Rare:30 | ||||
| chr14:75126289-75126654 | Common:1; Rare:82 | ||||
| chr14:75126700-75127314 | Common:6; Rare:180 | ||||
| chr14:75147752-75147963 | Common:3; Rare:32 |