| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68310887-68311068 | Common:1; Rare:90 | ||||
| chr16:68539138-68539353 | Common:2; Rare:103 | ||||
| chr16:69132537-69132689 | Rare:62 | ||||
| chr16:69339559-69339822 | Common:1; Rare:106; Clinvar (benign):1 | ||||
| chr16:69424488-69424678 | Rare:53 | ||||
| chr16:69726442-69726792 | Common:3; Rare:93 | ||||
| chr16:70114127-70114376 | Common:3; Rare:89 | ||||
| chr16:70289431-70289780 | Common:3; Rare:143; Clinvar:1 | ||||
| chr16:70299137-70299237 | Rare:22 | ||||
| chr16:70346759-70346971 | Common:2; Rare:103 | ||||
| chr16:70523524-70523855 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71808754-71808876 | Common:1; Rare:66 | ||||
| chr16:71808992-71809348 | Common:3; Rare:114 | ||||
| chr16:71845874-71846029 | Common:2; Rare:55 | ||||
| chr16:71895254-71895574 | Common:2; Rare:123 |