| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:48553990-48554160 | Rare:34 | ||||
| chr16:48609778-48610359 | Common:3; Rare:196 | ||||
| chr16:50368797-50369190 | Common:7; Rare:123 | ||||
| chr16:50693328-50693638 | Common:3; Rare:99 | ||||
| chr16:50741669-50741874 | Common:3; Rare:57 | ||||
| chr16:50742264-50742464 | Common:2; Rare:56 | ||||
| chr16:53054904-53055058 | Common:1; Rare:31 | ||||
| chr16:53130978-53131052 | Rare:24 | ||||
| chr16:53703797-53704227 | Common:1; Rare:134; Clinvar:5; Clinvar (benign):2 | ||||
| chr16:54286191-54286393 | Common:3; Rare:45 | ||||
| chr16:54286663-54286975 | Common:2; Rare:86 | ||||
| chr16:54930576-54930894 | Common:1; Rare:83 | ||||
| chr16:55566508-55567422 | Common:2; Rare:235 | ||||
| chr16:56451139-56451760 | Common:5; Rare:205 | ||||
| chr16:56519774-56519891 | Rare:50; Clinvar:4; Clinvar (pathogenic):1 |