| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30958576-30958784 | Rare:55 | ||||
| chr16:31123825-31123959 | Rare:29 | ||||
| chr16:31181234-31181454 | Rare:70 | ||||
| chr16:31189112-31189395 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr16:31191586-31191866 | Common:1; Rare:112; Clinvar:5; Clinvar (benign):1 | ||||
| chr16:31569707-31569972 | Common:1; Rare:51 | ||||
| chr16:31917415-31917486 | Rare:9 | ||||
| chr16:46660465-46660813 | Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46697236-46697475 | Common:1; Rare:45 | ||||
| chr16:46723712-46723804 | Rare:19 | ||||
| chr16:46925747-46926003 | Common:1; Rare:53 | ||||
| chr16:46963943-46963975 | Rare:4 | ||||
| chr16:47195842-47196209 | Common:1; Rare:56 | ||||
| chr16:47211843-47211933 | Rare:19 | ||||
| chr16:47295920-47296041 | Rare:20 |