| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74922764-74922808 | Rare:8 | ||||
| chr14:74923194-74923368 | Common:1; Rare:51 | ||||
| chr14:74955561-74955790 | Common:1; Rare:52 | ||||
| chr14:75002532-75003018 | Common:1; Rare:148; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75051095-75051280 | Rare:51 | ||||
| chr14:75051307-75051549 | Common:3; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75063676-75063743 | Rare:8 | ||||
| chr14:75063780-75063803 | Rare:3 | ||||
| chr14:75063955-75064218 | Common:1; Rare:74 | ||||
| chr14:75069197-75069329 | Common:1; Rare:54 | ||||
| chr14:75069361-75069772 | Common:2; Rare:102 | ||||
| chr14:75126736-75126895 | Common:2; Rare:45 | ||||
| chr14:75126904-75127505 | Common:4; Rare:167 | ||||
| chr14:75127583-75127692 | Common:1; Rare:22 | ||||
| chr14:75147747-75147938 | Common:3; Rare:29 |