| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:65412265-65412519 | Common:1; Rare:80 | ||||
| chr14:65412521-65412823 | Common:2; Rare:92 | ||||
| chr14:65412860-65413046 | Common:3; Rare:48 | ||||
| chr14:65413498-65413618 | Common:1; Rare:35 | ||||
| chr14:66506984-66507212 | Common:1; Rare:49 | ||||
| chr14:66507304-66507704 | Common:1; Rare:91 | ||||
| chr14:66507712-66508232 | Common:1; Rare:208 | ||||
| chr14:66508310-66508582 | Rare:91; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:66508903-66509098 | Common:1; Rare:62 | ||||
| chr14:67240618-67240765 | Rare:20 | ||||
| chr14:67241028-67241605 | Common:3; Rare:145 | ||||
| chr14:67241837-67242061 | Rare:40 | ||||
| chr14:67359413-67359552 | Common:1; Rare:26 | ||||
| chr14:67359681-67360110 | Common:1; Rare:139 | ||||
| chr14:67360224-67360585 | Common:2; Rare:108 |