| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67935647-67935848 | Rare:59 | ||||
| chr16:67968571-67968863 | Common:2; Rare:97 | ||||
| chr16:68023183-68023302 | Common:2; Rare:43 | ||||
| chr16:68264365-68264564 | Rare:62 | ||||
| chr16:68310927-68311062 | Common:1; Rare:65 | ||||
| chr16:68539158-68539338 | Common:2; Rare:88 | ||||
| chr16:69132498-69132671 | Rare:64 | ||||
| chr16:69339542-69339821 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:69762210-69762367 | Common:1; Rare:48 | ||||
| chr16:70523532-70523861 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
| chr16:71895254-71895574 | Common:2; Rare:123 | ||||
| chr16:72093598-72093934 | Rare:79 | ||||
| chr16:74296723-74296932 | Rare:89 | ||||
| chr16:74607082-74607197 | Rare:60 | ||||
| chr16:74666822-74667080 | Common:4; Rare:97 |