| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4474497-4474785 | Common:3; Rare:77 | ||||
| chr16:4476192-4476547 | Common:3; Rare:122 | ||||
| chr16:4538392-4538610 | Common:2; Rare:73 | ||||
| chr16:4538714-4538884 | Rare:65 | ||||
| chr16:4614787-4615134 | Common:1; Rare:119 | ||||
| chr16:4616095-4616673 | Common:1; Rare:158 | ||||
| chr16:4624306-4624894 | Common:1; Rare:189 | ||||
| chr16:4625021-4625227 | Common:2; Rare:74 | ||||
| chr16:4625374-4625550 | Common:1; Rare:55 | ||||
| chr16:4693394-4693797 | Common:4; Rare:175 | ||||
| chr16:4734098-4734330 | Common:1; Rare:91 | ||||
| chr16:4734338-4734576 | Rare:74 | ||||
| chr16:4734616-4735047 | Common:3; Rare:121 | ||||
| chr16:4767083-4767454 | Common:3; Rare:116 | ||||
| chr16:4802135-4802438 | Common:1; Rare:160; Clinvar (benign):3; Clinvar (pathogenic):1 |