| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74084352-74084641 | Common:2; Rare:82 | ||||
| chr14:74084788-74085060 | Common:3; Rare:97 | ||||
| chr14:74085335-74085532 | Common:2; Rare:30 | ||||
| chr14:74085971-74086117 | Common:1; Rare:26 | ||||
| chr14:74302874-74303188 | Common:3; Rare:121; Clinvar (benign):3 | ||||
| chr14:74493263-74493859 | Common:4; Rare:197; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74712988-74713250 | Common:1; Rare:134 | ||||
| chr14:74763027-74763442 | Rare:112 | ||||
| chr14:74881564-74882005 | Common:1; Rare:146 | ||||
| chr14:74882337-74882424 | Common:2; Rare:25 | ||||
| chr14:74955568-74955795 | Common:1; Rare:50 | ||||
| chr14:75002444-75003026 | Common:1; Rare:168; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75051159-75051234 | Rare:22 | ||||
| chr14:75051300-75051526 | Common:3; Rare:50; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75063735-75063759 | Rare:6 |