| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2475007-2475165 | Rare:55; Clinvar (benign):2 | ||||
| chr16:2682425-2682543 | Rare:53 | ||||
| chr16:2752567-2752704 | Common:1; Rare:55 | ||||
| chr16:3112491-3112612 | Common:1; Rare:30 | ||||
| chr16:3305345-3305514 | Common:2; Rare:57 | ||||
| chr16:3400967-3401251 | Common:6; Rare:103 | ||||
| chr16:3443450-3443725 | Common:3; Rare:90 | ||||
| chr16:3611575-3611761 | Rare:77 | ||||
| chr16:3717517-3717635 | Rare:59 | ||||
| chr16:4425766-4425879 | Common:1; Rare:53 | ||||
| chr16:4476270-4476481 | Common:3; Rare:79 | ||||
| chr16:4847244-4847436 | Common:1; Rare:82 | ||||
| chr16:5033920-5033961 | Rare:16 | ||||
| chr16:5097783-5098016 | Common:4; Rare:71 | ||||
| chr16:8797601-8797889 | Common:1; Rare:113; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |