| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49778259-49778470 | Common:1; Rare:48 | ||||
| chr14:49892971-49893136 | Rare:66 | ||||
| chr14:50312146-50312376 | Rare:101 | ||||
| chr14:50532509-50532606 | Common:2; Rare:31 | ||||
| chr14:50668327-50668573 | Common:4; Rare:97 | ||||
| chr14:50944276-50944600 | Common:5; Rare:115; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:51240009-51240295 | Common:2; Rare:98 | ||||
| chr14:51651636-51651968 | Common:4; Rare:93 | ||||
| chr14:52069038-52069215 | Common:2; Rare:35 | ||||
| chr14:52314120-52314319 | Common:1; Rare:55 | ||||
| chr14:52695510-52695862 | Common:1; Rare:99 | ||||
| chr14:52707050-52707298 | Common:1; Rare:102 | ||||
| chr14:52791418-52791889 | Common:3; Rare:148 | ||||
| chr14:52951018-52951395 | Common:4; Rare:132 | ||||
| chr14:54902819-54902935 | Rare:31; Clinvar (benign):1 |