| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11976618-11976772 | Common:2; Rare:58 | ||||
| chr16:14630195-14630413 | Rare:95 | ||||
| chr16:14632705-14632989 | Common:1; Rare:98 | ||||
| chr16:15094237-15094367 | Common:1; Rare:65 | ||||
| chr16:15857005-15857173 | Common:2; Rare:41; Clinvar (benign):2 | ||||
| chr16:18790246-18790460 | Common:4; Rare:80 | ||||
| chr16:18801449-18801813 | Common:3; Rare:126 | ||||
| chr16:19067413-19067702 | Common:5; Rare:117; Clinvar:1 | ||||
| chr16:19067773-19067925 | Common:2; Rare:39 | ||||
| chr16:20763903-20764038 | Common:2; Rare:19 | ||||
| chr16:20806338-20806663 | Rare:103 | ||||
| chr16:21158488-21158740 | Common:2; Rare:70 | ||||
| chr16:21652594-21652818 | Rare:50 | ||||
| chr16:21953024-21953391 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr16:22206544-22206578 | Rare:9 |