| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3400967-3401235 | Common:6; Rare:98 | ||||
| chr16:3443450-3443738 | Common:3; Rare:98 | ||||
| chr16:3611567-3611784 | Rare:94; Clinvar:1 | ||||
| chr16:4425763-4425907 | Common:1; Rare:77 | ||||
| chr16:4476273-4476459 | Common:3; Rare:68 | ||||
| chr16:4538386-4538594 | Common:3; Rare:68 | ||||
| chr16:4538741-4538883 | Rare:57 | ||||
| chr16:4614853-4615096 | Common:1; Rare:73 | ||||
| chr16:4734199-4734521 | Common:1; Rare:104 | ||||
| chr16:4767134-4767349 | Common:1; Rare:73 | ||||
| chr16:5033926-5033976 | Rare:17 | ||||
| chr16:5097737-5098016 | Common:4; Rare:98 | ||||
| chr16:8797618-8797877 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8868971-8869267 | Common:4; Rare:132 | ||||
| chr16:10580573-10580878 | Common:2; Rare:105 |