| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:25257355-25257609 | Rare:87 | ||||
| chr16:27268712-27268872 | Common:1; Rare:57 | ||||
| chr16:27313456-27313616 | Common:2; Rare:36 | ||||
| chr16:27313804-27313993 | Common:2; Rare:52 | ||||
| chr16:27314410-27314670 | Common:1; Rare:51 | ||||
| chr16:27549846-27550177 | Common:2; Rare:130 | ||||
| chr16:28491907-28492149 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28494356-28494688 | Rare:68 | ||||
| chr16:28538795-28539079 | Common:1; Rare:78 | ||||
| chr16:28554149-28554464 | Common:5; Rare:103 | ||||
| chr16:28822686-28822734 | Rare:19 | ||||
| chr16:28824317-28824511 | Common:2; Rare:73 | ||||
| chr16:28843751-28844126 | Rare:122; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:28844212-28844473 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:28844715-28845032 | Rare:107; Clinvar:2; Clinvar (benign):4 |