| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4425778-4425923 | Common:1; Rare:81 | ||||
| chr16:4476271-4476483 | Common:3; Rare:80 | ||||
| chr16:4538394-4538629 | Common:3; Rare:82 | ||||
| chr16:4538719-4538874 | Rare:60 | ||||
| chr16:4693476-4693735 | Common:2; Rare:114 | ||||
| chr16:4734160-4734534 | Common:1; Rare:124 | ||||
| chr16:4767126-4767308 | Common:1; Rare:63 | ||||
| chr16:4802594-4802781 | Rare:66; Clinvar:5 | ||||
| chr16:4847254-4847441 | Common:1; Rare:80 | ||||
| chr16:5033926-5033968 | Rare:13 | ||||
| chr16:5071749-5071849 | Rare:43; Clinvar (benign):1 | ||||
| chr16:5097737-5098014 | Common:4; Rare:98 | ||||
| chr16:8621620-8621712 | Common:1; Rare:36 | ||||
| chr16:8797631-8797885 | Rare:100; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8861730-8861811 | Common:1; Rare:28 |