| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50561075-50561247 | Rare:30 | ||||
| chr14:50668291-50668563 | Common:4; Rare:101 | ||||
| chr14:50944162-50944809 | Common:9; Rare:199; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr14:50944914-50945108 | Common:2; Rare:39 | ||||
| chr14:50945141-50945174 | Rare:3 | ||||
| chr14:51488674-51489288 | Common:3; Rare:114 | ||||
| chr14:51489295-51489454 | Common:1; Rare:36 | ||||
| chr14:51554452-51554685 | Rare:49 | ||||
| chr14:51651745-51651988 | Common:4; Rare:69 | ||||
| chr14:51989488-51989699 | Common:2; Rare:88 | ||||
| chr14:52552491-52552843 | Common:1; Rare:108 | ||||
| chr14:52646210-52646464 | Rare:54 | ||||
| chr14:52695367-52695773 | Common:1; Rare:114 | ||||
| chr14:52695848-52696021 | Common:1; Rare:55 | ||||
| chr14:52707080-52707225 | Common:1; Rare:60 |