| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27268713-27268869 | Common:1; Rare:56 | ||||
| chr16:27313655-27313974 | Common:7; Rare:85 | ||||
| chr16:27549846-27550182 | Common:2; Rare:132 | ||||
| chr16:28111688-28111969 | Common:2; Rare:64 | ||||
| chr16:28538834-28538863 | Rare:9 | ||||
| chr16:28553825-28553994 | Common:1; Rare:56 | ||||
| chr16:28623329-28623436 | Rare:40 | ||||
| chr16:28822576-28822769 | Rare:74 | ||||
| chr16:28822924-28823280 | Common:4; Rare:121 | ||||
| chr16:28823964-28824159 | Common:2; Rare:59 | ||||
| chr16:28843818-28844099 | Rare:93; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:28844532-28845048 | Common:2; Rare:161; Clinvar:3; Clinvar (benign):7 | ||||
| chr16:28846234-28846696 | Common:2; Rare:153; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863462-28863575 | Rare:23 | ||||
| chr16:28863721-28863883 | Common:1; Rare:48 |