| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95533507-95533630 | Rare:49 | ||||
| chr14:95534593-95534694 | Rare:35 | ||||
| chr14:95534749-95535049 | Common:4; Rare:89; Clinvar (benign):1 | ||||
| chr14:96363286-96363552 | Common:1; Rare:89 | ||||
| chr14:96502301-96502570 | Common:1; Rare:118 | ||||
| chr14:99480728-99481035 | Common:2; Rare:115 | ||||
| chr14:99580147-99580220 | Rare:18 | ||||
| chr14:99737586-99737832 | Common:2; Rare:62 | ||||
| chr14:100066354-100066441 | Common:1; Rare:13 | ||||
| chr14:100159621-100159953 | Common:3; Rare:85 | ||||
| chr14:100238558-100238848 | Common:2; Rare:85 | ||||
| chr14:100238978-100239299 | Common:1; Rare:127 | ||||
| chr14:100306439-100306702 | Common:3; Rare:93 | ||||
| chr14:100375311-100375758 | Common:4; Rare:74 | ||||
| chr14:100376259-100376521 | Common:3; Rare:84 |