| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31508381-31508490 | Common:4; Rare:43 | ||||
| chr16:46621325-46621474 | Rare:54 | ||||
| chr16:46689134-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689489-46689720 | Common:2; Rare:95; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46789926-46790124 | Common:5; Rare:49 | ||||
| chr16:46973603-46973819 | Rare:101 | ||||
| chr16:47461032-47461350 | Common:2; Rare:114; Clinvar (benign):2 | ||||
| chr16:48385283-48385520 | Common:3; Rare:92 | ||||
| chr16:50681306-50681438 | Rare:30 | ||||
| chr16:53054874-53055048 | Common:1; Rare:42 | ||||
| chr16:53098996-53099225 | Rare:43 | ||||
| chr16:53208321-53208504 | Rare:37 | ||||
| chr16:53503184-53503530 | Common:9; Rare:107 | ||||
| chr16:53703817-53704206 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54930573-54930733 | Common:1; Rare:42 |