| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8621568-8621782 | Common:1; Rare:86 | ||||
| chr16:8674380-8674714 | Common:1; Rare:113; Clinvar:3 | ||||
| chr16:8797513-8797937 | Common:3; Rare:175; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8798064-8798106 | Common:1; Rare:10 | ||||
| chr16:8868176-8868351 | Common:2; Rare:45 | ||||
| chr16:8868379-8868480 | Rare:25 | ||||
| chr16:8868619-8868794 | Rare:48 | ||||
| chr16:8868923-8869331 | Common:6; Rare:183 | ||||
| chr16:8962490-8962923 | Common:5; Rare:148 | ||||
| chr16:8963814-8964171 | Common:3; Rare:134 | ||||
| chr16:8964315-8964343 | Rare:10 | ||||
| chr16:9091069-9091265 | Common:2; Rare:86 | ||||
| chr16:9091549-9091695 | Common:1; Rare:73 | ||||
| chr16:9092202-9092404 | Rare:75 | ||||
| chr16:10385825-10386108 | Rare:103 |