| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75278245-75279143 | Common:6; Rare:222 | ||||
| chr14:75279343-75279656 | Common:1; Rare:62 | ||||
| chr14:75427710-75427831 | Rare:23 | ||||
| chr14:75427857-75428138 | Rare:67 | ||||
| chr14:75428178-75428339 | Common:1; Rare:52 | ||||
| chr14:75428340-75428609 | Common:1; Rare:59 | ||||
| chr14:75578453-75578722 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr14:75660783-75661003 | Rare:60 | ||||
| chr14:75661052-75661570 | Common:7; Rare:129 | ||||
| chr14:75661657-75661729 | Rare:16 | ||||
| chr14:75982249-75982401 | Common:1; Rare:38 | ||||
| chr14:75982485-75982581 | Common:1; Rare:21 | ||||
| chr14:75982589-75982639 | Rare:5 | ||||
| chr14:75982783-75982836 | Common:1; Rare:13 | ||||
| chr14:75985704-75985824 | Rare:65; Clinvar:3; Clinvar (pathogenic):2 |