| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28491938-28492127 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28538795-28539086 | Common:1; Rare:80 | ||||
| chr16:28597016-28597119 | Common:2; Rare:33 | ||||
| chr16:28822539-28822734 | Common:1; Rare:68 | ||||
| chr16:28822896-28823125 | Common:3; Rare:65 | ||||
| chr16:28824126-28824507 | Common:3; Rare:126 | ||||
| chr16:28846216-28846698 | Common:2; Rare:162; Clinvar:7; Clinvar (benign):6 | ||||
| chr16:28879887-28880045 | Common:3; Rare:47 | ||||
| chr16:28925167-28925266 | Rare:26 | ||||
| chr16:28926080-28926104 | Rare:7 | ||||
| chr16:28974658-28974813 | Rare:70 | ||||
| chr16:29454130-29454551 | |||||
| chr16:29678822-29679198 | Common:1; Rare:89 | ||||
| chr16:29790513-29790788 | Common:1; Rare:109; Clinvar (benign):2 | ||||
| chr16:29805482-29805688 | Common:2; Rare:96 |