| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73950035-73950355 | Common:6; Rare:141; Clinvar (benign):5 | ||||
| chr14:74019256-74019467 | Common:1; Rare:80 | ||||
| chr14:74084390-74084987 | Common:9; Rare:175 | ||||
| chr14:74493248-74493788 | Common:4; Rare:173; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74713036-74713213 | Rare:100 | ||||
| chr14:74763105-74763404 | Rare:90 | ||||
| chr14:74881831-74881964 | Rare:56 | ||||
| chr14:75002669-75002982 | Common:1; Rare:105; Clinvar:2 | ||||
| chr14:75127001-75127110 | Rare:33 | ||||
| chr14:75427707-75427758 | Rare:10 | ||||
| chr14:75660787-75660969 | Rare:48 | ||||
| chr14:75661168-75661330 | Common:2; Rare:44 | ||||
| chr14:75985709-75985799 | Rare:42; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:76151770-76151991 | Rare:77 | ||||
| chr14:76762638-76762775 | Rare:37 |