| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50668152-50668570 | Common:25; Rare:728 | ||||
| chr14:50668490-50668990 | Common:25; Rare:376 | ||||
| chr14:50821583-50821984 | Common:2; Rare:211 | ||||
| chr14:50830530-50830850 | Common:2; Rare:78 | ||||
| chr14:50830960-50831430 | Common:4; Rare:290 | ||||
| chr14:50944324-50944790 | Common:27; Rare:587; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr14:51239830-51240522 | Common:18; Rare:901 | ||||
| chr14:51651220-51651540 | Common:3; Rare:93 | ||||
| chr14:51651500-51652291 | Common:17; Rare:434 | ||||
| chr14:51989262-51989662 | Common:10; Rare:463 | ||||
| chr14:52552468-52552902 | Common:5; Rare:617 | ||||
| chr14:52694729-52695310 | Common:2; Rare:118 | ||||
| chr14:52695500-52696194 | Common:7; Rare:531 | ||||
| chr14:52706928-52707328 | Common:10; Rare:719 | ||||
| chr14:52729819-52730266 | Common:8; Rare:502 |