| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8720444-8720765 | Common:2; Rare:88 | ||||
| chr16:8797624-8797873 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:8868977-8869283 | Common:4; Rare:137 | ||||
| chr16:10580569-10580846 | Common:2; Rare:94 | ||||
| chr16:10944326-10944607 | Common:1; Rare:84 | ||||
| chr16:11587167-11587313 | Common:1; Rare:34 | ||||
| chr16:11851511-11851635 | Rare:61 | ||||
| chr16:11915900-11916227 | Common:2; Rare:131 | ||||
| chr16:14630200-14630404 | Rare:89 | ||||
| chr16:14632722-14632981 | Common:1; Rare:88 | ||||
| chr16:15094239-15094446 | Common:1; Rare:99 | ||||
| chr16:15642609-15642811 | Common:2; Rare:60 | ||||
| chr16:15650046-15650283 | Common:1; Rare:121 | ||||
| chr16:15888587-15888708 | Common:1; Rare:57 | ||||
| chr16:18790200-18790484 | Common:5; Rare:98 |