| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56191971-56192314 | Common:1; Rare:66; Clinvar (benign):3 | ||||
| chr16:56451306-56451605 | Common:1; Rare:98 | ||||
| chr16:56519991-56520150 | Common:4; Rare:60; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56657859-56657970 | Common:1; Rare:37 | ||||
| chr16:56729941-56730189 | Common:1; Rare:60 | ||||
| chr16:56931934-56932147 | Common:1; Rare:104 | ||||
| chr16:57185923-57186342 | Common:2; Rare:118 | ||||
| chr16:57244976-57245185 | Common:3; Rare:69 | ||||
| chr16:57447371-57447508 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57639355-57639509 | Rare:32; Clinvar (pathogenic):1 | ||||
| chr16:58001318-58001429 | Rare:26 | ||||
| chr16:58129263-58129540 | Common:2; Rare:90 | ||||
| chr16:58249825-58250017 | Rare:52 | ||||
| chr16:58515430-58515533 | Common:1; Rare:42 | ||||
| chr16:62036416-62036562 | Rare:34 |