| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75002627-75003026 | Common:1; Rare:132; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75051409-75051484 | Common:1; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:75063988-75064136 | Common:1; Rare:40 | ||||
| chr14:75126945-75127106 | Rare:52 | ||||
| chr14:75279056-75279142 | Rare:24 | ||||
| chr14:75279366-75279660 | Common:1; Rare:56 | ||||
| chr14:75280184-75280513 | Common:1; Rare:69 | ||||
| chr14:75427956-75428203 | Rare:53 | ||||
| chr14:75578309-75578728 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr14:75578734-75578996 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:75579504-75579669 | Common:3; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:75641086-75641231 | Common:1; Rare:35 | ||||
| chr14:75660789-75661327 | Common:4; Rare:131 | ||||
| chr14:76762653-76762906 | Rare:83 | ||||
| chr14:77097991-77098366 | Rare:119 |