| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96502711-96502971 | Common:4; Rare:79 | ||||
| chr14:96502992-96503242 | Rare:64 | ||||
| chr14:96797193-96797495 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:96797589-96797853 | Common:3; Rare:67 | ||||
| chr14:99270675-99270829 | Rare:28 | ||||
| chr14:99480381-99480471 | Rare:28 | ||||
| chr14:99480731-99481032 | Common:2; Rare:113 | ||||
| chr14:99481069-99481525 | Common:1; Rare:124 | ||||
| chr14:99481824-99481992 | Rare:34 | ||||
| chr14:99579816-99580116 | Common:11; Rare:81 | ||||
| chr14:99603977-99604693 | Common:4; Rare:208 | ||||
| chr14:99683830-99684360 | Common:1; Rare:113 | ||||
| chr14:99793118-99793559 | Rare:117 | ||||
| chr14:99793655-99793884 | Rare:52 | ||||
| chr14:99793899-99793940 | Rare:6 |