| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95535348-95535354 | Rare:3 | ||||
| chr14:96204732-96204839 | Common:1; Rare:32 | ||||
| chr14:96363276-96363552 | Common:1; Rare:91 | ||||
| chr14:96502301-96502521 | Common:1; Rare:97 | ||||
| chr14:99480764-99481013 | Common:2; Rare:96 | ||||
| chr14:100065295-100065439 | Rare:23 | ||||
| chr14:100238558-100238831 | Common:2; Rare:81 | ||||
| chr14:100375331-100375758 | Common:4; Rare:71 | ||||
| chr14:100376268-100376514 | Common:3; Rare:81 | ||||
| chr14:101809724-101810034 | Rare:75 | ||||
| chr14:101810287-101810453 | Common:2; Rare:34 | ||||
| chr14:101823684-101823875 | Rare:39 | ||||
| chr14:101964321-101964662 | Common:4; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102086978-102087314 | Common:4; Rare:134 | ||||
| chr14:102087550-102087623 | Common:1; Rare:20 |