| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50532443-50532716 | Common:3; Rare:81 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 | ||||
| chr14:50944200-50944595 | Common:6; Rare:140; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr14:50944914-50945034 | Common:1; Rare:24 | ||||
| chr14:51240009-51240306 | Common:2; Rare:106 | ||||
| chr14:51651656-51652148 | Common:6; Rare:138 | ||||
| chr14:51989446-51989699 | Common:2; Rare:96 | ||||
| chr14:52552481-52552837 | Common:1; Rare:110 | ||||
| chr14:52707082-52707253 | Common:1; Rare:76 | ||||
| chr14:52730267-52730531 | Common:2; Rare:85 | ||||
| chr14:52791418-52791798 | Common:2; Rare:123 | ||||
| chr14:52951011-52951423 | Common:4; Rare:146 | ||||
| chr14:54396711-54397077 | Common:2; Rare:102 | ||||
| chr14:54441249-54441751 | Common:1; Rare:154 | ||||
| chr14:55027031-55027432 | Common:4; Rare:100 |