| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8797612-8797895 | Common:1; Rare:113; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:10744069-10744324 | Common:1; Rare:92 | ||||
| chr16:11586893-11587083 | Common:3; Rare:52 | ||||
| chr16:11598457-11598722 | Common:3; Rare:74 | ||||
| chr16:11742722-11743093 | Common:2; Rare:153 | ||||
| chr16:11797166-11797563 | Common:4; Rare:155 | ||||
| chr16:12803733-12803776 | Common:1; Rare:20 | ||||
| chr16:14630185-14630444 | Rare:108 | ||||
| chr16:14632701-14632995 | Common:1; Rare:104 | ||||
| chr16:15094199-15094439 | Common:3; Rare:120 | ||||
| chr16:15643031-15643267 | Rare:73 | ||||
| chr16:17369616-17369828 | Common:1; Rare:31 | ||||
| chr16:20763918-20764056 | Common:2; Rare:22 | ||||
| chr16:20806437-20806610 | Rare:58 | ||||
| chr16:20900797-20900828 | Common:1; Rare:11 |