| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4693456-4693732 | Common:2; Rare:116 | ||||
| chr16:4734199-4734307 | Common:1; Rare:38 | ||||
| chr16:4870075-4870542 | Common:4; Rare:178 | ||||
| chr16:4892264-4892298 | Rare:3 | ||||
| chr16:4893211-4893612 | Common:1; Rare:159 | ||||
| chr16:4936985-4937362 | Common:6; Rare:138 | ||||
| chr16:5097738-5098007 | Common:4; Rare:97 | ||||
| chr16:8797627-8797877 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:9091415-9091656 | Rare:95 | ||||
| chr16:10580123-10580312 | Common:1; Rare:50 | ||||
| chr16:11414569-11414747 | Common:1; Rare:43 | ||||
| chr16:11586896-11587024 | Common:1; Rare:39 | ||||
| chr16:11851406-11851635 | Common:1; Rare:118 | ||||
| chr16:11895060-11895375 | Rare:71 | ||||
| chr16:11915370-11915763 | Common:6; Rare:158 |