| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73569054-73569319 | Rare:123 | ||||
| chr14:73644870-73645027 | Common:3; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73760028-73760580 | Common:5; Rare:136 | ||||
| chr14:73787116-73787351 | Common:3; Rare:153 | ||||
| chr14:73851592-73851990 | Common:4; Rare:113 | ||||
| chr14:73886768-73886913 | Common:4; Rare:89 | ||||
| chr14:73950053-73950348 | Common:10; Rare:222; Clinvar (benign):6 | ||||
| chr14:73996110-73996650 | Common:2; Rare:122 | ||||
| chr14:74019134-74019452 | Common:4; Rare:189 | ||||
| chr14:74084396-74084786 | Common:11; Rare:160 | ||||
| chr14:74296130-74296360 | Common:2; Rare:54; Clinvar (pathogenic):1 | ||||
| chr14:74302915-74303136 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chr14:74493250-74493791 | Common:7; Rare:251; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr14:74713015-74713203 | Common:2; Rare:211 | ||||
| chr14:74762990-74763412 | Rare:189 |