| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:70454133-70454350 | Common:2; Rare:40 | ||||
| chr16:70454370-70454744 | Common:5; Rare:126 | ||||
| chr16:70523124-70523173 | Rare:11 | ||||
| chr16:70523190-70523327 | Common:2; Rare:32 | ||||
| chr16:70523451-70523876 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70523971-70524060 | Rare:21 | ||||
| chr16:70524191-70524543 | Common:2; Rare:92 | ||||
| chr16:70524566-70524659 | Common:3; Rare:15 | ||||
| chr16:70685103-70685591 | Common:6; Rare:102 | ||||
| chr16:70685786-70685922 | Rare:43 | ||||
| chr16:70685970-70686319 | Common:3; Rare:124 | ||||
| chr16:70800435-70800623 | Common:2; Rare:29 | ||||
| chr16:70801027-70801373 | Common:3; Rare:108 | ||||
| chr16:71230655-71230831 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr16:71289047-71289225 | Common:1; Rare:46 |