| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3443449-3443640 | Common:2; Rare:58 | ||||
| chr16:3457914-3458161 | Common:2; Rare:114 | ||||
| chr16:3611561-3611810 | Rare:107; Clinvar:1 | ||||
| chr16:3717513-3717643 | Rare:65 | ||||
| chr16:4272747-4272984 | Common:1; Rare:61 | ||||
| chr16:4273053-4273221 | Rare:50 | ||||
| chr16:4425763-4425892 | Common:1; Rare:63 | ||||
| chr16:4476270-4476481 | Common:3; Rare:79 | ||||
| chr16:4538390-4538634 | Common:4; Rare:83 | ||||
| chr16:4668386-4668428 | Rare:14 | ||||
| chr16:4734142-4734552 | Common:1; Rare:134 | ||||
| chr16:4767124-4767330 | Common:1; Rare:69 | ||||
| chr16:4847244-4847471 | Common:1; Rare:100 | ||||
| chr16:5033920-5034006 | Rare:31 | ||||
| chr16:8797579-8797942 | Common:3; Rare:151; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 |