| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75433435-75433805 | Common:4; Rare:112 | ||||
| chr16:75566219-75566461 | Common:1; Rare:124 | ||||
| chr16:75623208-75623384 | Common:4; Rare:66 | ||||
| chr16:75647581-75647905 | Common:4; Rare:157; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648040-75648280 | Rare:98 | ||||
| chr16:75648467-75648572 | Rare:38 | ||||
| chr16:75648609-75648663 | Rare:26 | ||||
| chr16:77190674-77191021 | Common:12; Rare:116 | ||||
| chr16:77191588-77191909 | Common:2; Rare:103 | ||||
| chr16:81006416-81006558 | Rare:39 | ||||
| chr16:81006808-81007280 | Common:4; Rare:160 | ||||
| chr16:82170193-82170409 | Common:2; Rare:103 | ||||
| chr16:83807885-83808119 | Common:1; Rare:83 | ||||
| chr16:83808383-83808721 | Common:1; Rare:109 | ||||
| chr16:83953155-83953347 | Common:2; Rare:82 |