| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68264430-68264564 | Rare:46 | ||||
| chr16:68310922-68311062 | Common:1; Rare:67 | ||||
| chr16:68530038-68530138 | Common:4; Rare:46 | ||||
| chr16:68539135-68539353 | Common:2; Rare:104 | ||||
| chr16:69132541-69132666 | Rare:51 | ||||
| chr16:69311097-69311414 | Rare:93 | ||||
| chr16:69339551-69339807 | Rare:101; Clinvar (benign):1 | ||||
| chr16:69726446-69726768 | Common:3; Rare:82 | ||||
| chr16:69762222-69762381 | Common:1; Rare:47 | ||||
| chr16:70114124-70114385 | Common:3; Rare:96 | ||||
| chr16:70299092-70299220 | Common:1; Rare:24 | ||||
| chr16:70346803-70346937 | Common:1; Rare:68 | ||||
| chr16:70523539-70523837 | Common:3; Rare:92 | ||||
| chr16:71289342-71289693 | Common:3; Rare:117 | ||||
| chr16:71808828-71808860 | Common:1; Rare:9 |