| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:99480769-99481014 | Common:2; Rare:95 | ||||
| chr14:100238539-100238754 | Common:3; Rare:69 | ||||
| chr14:100375394-100375763 | Common:3; Rare:56 | ||||
| chr14:100376268-100376521 | Common:3; Rare:84 | ||||
| chr14:100726721-100727135 | Common:1; Rare:115 | ||||
| chr14:101809736-101809893 | Rare:30 | ||||
| chr14:102083544-102083982 | Common:3; Rare:178 | ||||
| chr14:102139667-102139935 | Rare:94 | ||||
| chr14:102305131-102305310 | Common:1; Rare:61 | ||||
| chr14:102362858-102363092 | Rare:105 | ||||
| chr14:103333899-103334252 | Common:3; Rare:146 | ||||
| chr14:103529074-103529205 | Common:1; Rare:35 | ||||
| chr14:103562620-103563059 | Common:8; Rare:174; Clinvar (benign):5 | ||||
| chr14:103629082-103629452 | Common:3; Rare:148 | ||||
| chr14:103715437-103715847 | Common:1; Rare:136 |