| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93333078-93333189 | Common:1; Rare:46 | ||||
| chr14:94081150-94081362 | Common:3; Rare:70 | ||||
| chr14:95157434-95157715 | Common:4; Rare:103 | ||||
| chr14:95534566-95534701 | Rare:55 | ||||
| chr14:96363286-96363552 | Common:1; Rare:89 | ||||
| chr14:96502286-96502460 | Rare:66 | ||||
| chr14:99480786-99481013 | Common:2; Rare:88 | ||||
| chr14:100238535-100238814 | Common:3; Rare:81 | ||||
| chr14:100376269-100376485 | Common:3; Rare:73 | ||||
| chr14:101809672-101809890 | Rare:43 | ||||
| chr14:101810298-101810372 | Rare:16 | ||||
| chr14:102139678-102139914 | Rare:80 | ||||
| chr14:102362862-102363089 | Rare:101 | ||||
| chr14:103333909-103334246 | Common:3; Rare:139 | ||||
| chr14:103562624-103563044 | Common:8; Rare:164; Clinvar (benign):5 |