| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73851638-73851983 | Common:4; Rare:104 | ||||
| chr14:73886785-73886911 | Common:2; Rare:42 | ||||
| chr14:73950053-73950348 | Common:6; Rare:134; Clinvar (benign):4 | ||||
| chr14:74019233-74019436 | Common:1; Rare:81 | ||||
| chr14:74084397-74084494 | Rare:34 | ||||
| chr14:74493215-74493781 | Common:4; Rare:184; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:74713052-74713218 | Rare:95 | ||||
| chr14:75002741-75003011 | Common:1; Rare:92; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75069405-75069680 | Common:2; Rare:71 | ||||
| chr14:75126945-75127128 | Rare:64 | ||||
| chr14:75147664-75147932 | Common:3; Rare:48 | ||||
| chr14:75176353-75176657 | Rare:93 | ||||
| chr14:75278376-75278620 | Common:1; Rare:55 | ||||
| chr14:75278916-75279128 | Common:1; Rare:66 | ||||
| chr14:75279627-75279765 | Rare:17 |