| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:72074031-72074218 | Common:1; Rare:45 | ||||
| chr16:72664968-72665145 | Rare:54 | ||||
| chr16:74302018-74302293 | Common:1; Rare:64 | ||||
| chr16:74368104-74368386 | Common:1; Rare:80 | ||||
| chr16:75376800-75376964 | Common:4; Rare:33 | ||||
| chr16:79598316-79598796 | Common:12; Rare:120 | ||||
| chr16:79598888-79599100 | Rare:49; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:84829361-84829514 | Common:1; Rare:38 | ||||
| chr16:84832414-84832526 | Common:2; Rare:24 | ||||
| chr16:84836532-84836573 | Rare:12 | ||||
| chr16:85563959-85564082 | Rare:36 | ||||
| chr16:87345207-87345390 | Common:2; Rare:56 | ||||
| chr16:87381507-87381620 | Rare:29 | ||||
| chr16:88086785-88087128 | Common:3; Rare:88 | ||||
| chr16:88233966-88234153 | Common:1; Rare:37 |