| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27549886-27550167 | Common:2; Rare:104 | ||||
| chr16:28491949-28492100 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28822594-28822749 | Rare:61 | ||||
| chr16:28822931-28823133 | Common:3; Rare:57 | ||||
| chr16:28823964-28824129 | Common:1; Rare:48 | ||||
| chr16:28824378-28824542 | Rare:62 | ||||
| chr16:28843788-28844299 | Common:1; Rare:164; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr16:28846271-28846729 | Common:2; Rare:146; Clinvar:5; Clinvar (benign):5 | ||||
| chr16:28863366-28863585 | Rare:46 | ||||
| chr16:28863685-28864056 | Common:3; Rare:101 | ||||
| chr16:28879885-28880043 | Common:3; Rare:48 | ||||
| chr16:28925105-28925412 | Rare:100 | ||||
| chr16:28925691-28925813 | Rare:20 | ||||
| chr16:28974676-28974792 | Rare:53 | ||||
| chr16:29790591-29790819 | Common:1; Rare:94; Clinvar (benign):2 |