| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73851814-73852105 | Common:8; Rare:87 | ||||
| chr14:73886600-73887028 | Common:4; Rare:127 | ||||
| chr14:73887056-73887215 | Common:1; Rare:32 | ||||
| chr14:73950105-73950392 | Common:5; Rare:124; Clinvar (benign):3 | ||||
| chr14:73950484-73950572 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chr14:74018966-74019326 | Common:3; Rare:108 | ||||
| chr14:74084337-74084578 | Common:1; Rare:76 | ||||
| chr14:74084763-74085049 | Common:3; Rare:100 | ||||
| chr14:74085369-74085509 | Common:1; Rare:25 | ||||
| chr14:74085970-74086121 | Common:1; Rare:27 | ||||
| chr14:74302859-74303219 | Common:3; Rare:130; Clinvar (benign):3 | ||||
| chr14:74493430-74493879 | Common:4; Rare:154; Clinvar (benign):4 | ||||
| chr14:74494110-74494145 | Rare:15 | ||||
| chr14:74712963-74713259 | Common:1; Rare:146 | ||||
| chr14:74763105-74763510 | Rare:116 |