| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74019250-74019452 | Common:1; Rare:75 | ||||
| chr14:74084361-74084619 | Common:2; Rare:77 | ||||
| chr14:74084817-74085011 | Common:1; Rare:72 | ||||
| chr14:74302905-74303099 | Common:1; Rare:78; Clinvar (benign):1 | ||||
| chr14:74493193-74493822 | Common:4; Rare:212; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74494119-74494329 | Rare:78; Clinvar (benign):1 | ||||
| chr14:74611947-74612248 | Common:1; Rare:73; Clinvar:6; Clinvar (benign):1 | ||||
| chr14:74612529-74612830 | Common:1; Rare:78 | ||||
| chr14:74713065-74713223 | Rare:83 | ||||
| chr14:74882320-74882624 | Common:3; Rare:81 | ||||
| chr14:75002732-75003106 | Common:1; Rare:128; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75126986-75127090 | Rare:36 | ||||
| chr14:75176524-75176661 | Rare:56 | ||||
| chr14:75278415-75278721 | Common:1; Rare:75 | ||||
| chr14:75278743-75279213 | Common:3; Rare:129 |