| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8797611-8797913 | Common:1; Rare:124; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:8868973-8869228 | Common:4; Rare:116 | ||||
| chr16:10385937-10386251 | Common:1; Rare:112 | ||||
| chr16:10580569-10580787 | Rare:71 | ||||
| chr16:10743793-10743869 | Rare:28 | ||||
| chr16:10944309-10944630 | Common:1; Rare:101 | ||||
| chr16:11586891-11587036 | Common:1; Rare:44 | ||||
| chr16:11851406-11851636 | Common:1; Rare:118 | ||||
| chr16:11915372-11915726 | Common:5; Rare:135 | ||||
| chr16:11915889-11916208 | Common:2; Rare:131 | ||||
| chr16:11976623-11976772 | Common:2; Rare:56 | ||||
| chr16:14071055-14071372 | Common:3; Rare:109 | ||||
| chr16:14632722-14632990 | Common:1; Rare:90 | ||||
| chr16:15094230-15094429 | Common:1; Rare:95 | ||||
| chr16:15643022-15643267 | Rare:74 |