| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66366403-66366754 | Common:3; Rare:75 | ||||
| chr16:66549778-66550021 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66552446-66552707 | Rare:110 | ||||
| chr16:66604246-66604280 | Common:1; Rare:6 | ||||
| chr16:66751496-66751938 | Common:3; Rare:136 | ||||
| chr16:66934256-66934706 | Common:1; Rare:137 | ||||
| chr16:67028989-67029124 | Rare:45 | ||||
| chr16:67109804-67109994 | Rare:61 | ||||
| chr16:67159884-67160009 | Rare:20 | ||||
| chr16:67170434-67170555 | Common:1; Rare:19 | ||||
| chr16:67183930-67184005 | Common:1; Rare:23 | ||||
| chr16:67227008-67227196 | Rare:80 | ||||
| chr16:67247447-67247727 | Rare:88 | ||||
| chr16:67277957-67278201 | Rare:41 | ||||
| chr16:67279250-67279555 | Common:1; Rare:85 |