| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56626007-56626315 | Common:2; Rare:68 | ||||
| chr16:56632257-56632672 | Common:2; Rare:117 | ||||
| chr16:56638533-56638691 | Rare:66 | ||||
| chr16:56657541-56657711 | Rare:39 | ||||
| chr16:56682071-56682543 | Common:8; Rare:136 | ||||
| chr16:56729945-56730185 | Common:1; Rare:57 | ||||
| chr16:56931928-56932177 | Common:2; Rare:128 | ||||
| chr16:56989474-56989605 | Common:1; Rare:27 | ||||
| chr16:57185736-57186340 | Common:3; Rare:162 | ||||
| chr16:57244913-57245262 | Common:3; Rare:122 | ||||
| chr16:57447360-57447514 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57619639-57619748 | Common:1; Rare:24 | ||||
| chr16:57619959-57620118 | Rare:35 | ||||
| chr16:57628395-57628722 | Common:4; Rare:78 | ||||
| chr16:57984933-57985172 | Common:5; Rare:72 |