| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73287294-73287418 | Rare:22 | ||||
| chr14:73569055-73569292 | Rare:57 | ||||
| chr14:73592025-73592163 | Common:2; Rare:53 | ||||
| chr14:73787121-73787379 | Common:2; Rare:88 | ||||
| chr14:73950053-73950330 | Common:6; Rare:118; Clinvar (benign):4 | ||||
| chr14:74019259-74019455 | Common:1; Rare:73 | ||||
| chr14:74493215-74493777 | Common:4; Rare:183; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74713074-74713207 | Rare:67 | ||||
| chr14:75002741-75002962 | Common:1; Rare:65; Clinvar:2 | ||||
| chr14:75069488-75069680 | Common:1; Rare:44 | ||||
| chr14:75127001-75127120 | Rare:38 | ||||
| chr14:75176505-75176937 | Common:1; Rare:114 | ||||
| chr14:75279862-75279894 | Rare:6 | ||||
| chr14:75578475-75578680 | Common:2; Rare:36; Clinvar (benign):1 | ||||
| chr14:75660819-75661314 | Common:4; Rare:119 |