| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95534710-95535002 | Common:3; Rare:80 | ||||
| chr14:95535343-95535378 | Rare:18 | ||||
| chr14:96363257-96363552 | Common:1; Rare:98 | ||||
| chr14:96391767-96392155 | Common:2; Rare:110 | ||||
| chr14:96502231-96502570 | Common:2; Rare:146 | ||||
| chr14:99480739-99481007 | Common:2; Rare:107 | ||||
| chr14:100019288-100019596 | Common:1; Rare:58 | ||||
| chr14:100238565-100238790 | Common:2; Rare:69 | ||||
| chr14:100375305-100375768 | Common:4; Rare:75 | ||||
| chr14:100376258-100376535 | Common:3; Rare:88 | ||||
| chr14:100568933-100569253 | Common:4; Rare:79 | ||||
| chr14:100569558-100569659 | Common:1; Rare:23 | ||||
| chr14:101809736-101810000 | Rare:57 | ||||
| chr14:101810287-101810321 | Rare:6 | ||||
| chr14:101964319-101964721 | Common:5; Rare:124; Clinvar:2; Clinvar (benign):3 |