| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2682367-2682598 | Rare:103 | ||||
| chr16:2777235-2777392 | Common:1; Rare:65 | ||||
| chr16:3112446-3112603 | Rare:43 | ||||
| chr16:3305397-3305518 | Common:1; Rare:42 | ||||
| chr16:3400975-3401246 | Common:6; Rare:97 | ||||
| chr16:3443469-3443737 | Common:3; Rare:92 | ||||
| chr16:3457914-3458076 | Common:2; Rare:79 | ||||
| chr16:3611572-3611794 | Rare:96 | ||||
| chr16:4371693-4371848 | Rare:55 | ||||
| chr16:4476315-4476467 | Rare:60 | ||||
| chr16:4538427-4538614 | Common:1; Rare:69 | ||||
| chr16:4693489-4693729 | Common:2; Rare:106 | ||||
| chr16:4734199-4734298 | Common:1; Rare:33 | ||||
| chr16:4767126-4767330 | Common:1; Rare:67 | ||||
| chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 |