| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73058477-73058650 | Common:2; Rare:59 | ||||
| chr14:73458497-73458873 | Common:5; Rare:102 | ||||
| chr14:73713260-73714036 | Common:2; Rare:214 | ||||
| chr14:73787114-73787319 | Common:1; Rare:75 | ||||
| chr14:73949834-73949955 | Common:3; Rare:39 | ||||
| chr14:73950111-73950362 | Common:5; Rare:109; Clinvar (benign):3 | ||||
| chr14:74019254-74019442 | Common:1; Rare:73 | ||||
| chr14:74493193-74493826 | Common:4; Rare:213; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74494031-74494339 | Rare:111; Clinvar (benign):2 | ||||
| chr14:74612511-74612777 | Common:1; Rare:70 | ||||
| chr14:74713070-74713217 | Rare:78 | ||||
| chr14:74835037-74835446 | Rare:83 | ||||
| chr14:74881623-74882016 | Common:1; Rare:142 | ||||
| chr14:75002871-75003421 | Rare:198; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:75069477-75069641 | Rare:44 |