| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1612044-1612360 | Common:2; Rare:106; Clinvar:1 | ||||
| chr16:1706056-1706286 | Common:1; Rare:67 | ||||
| chr16:1826785-1826975 | Common:3; Rare:62 | ||||
| chr16:1827179-1827241 | Rare:35 | ||||
| chr16:1941327-1941647 | Common:1; Rare:94 | ||||
| chr16:1943119-1943503 | Common:1; Rare:120 | ||||
| chr16:1959459-1959750 | Common:4; Rare:133 | ||||
| chr16:1964792-1964947 | Common:8; Rare:70 | ||||
| chr16:1971932-1972134 | Common:1; Rare:60 | ||||
| chr16:2047784-2048038 | Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2268063-2268186 | Common:1; Rare:61 | ||||
| chr16:2340766-2341065 | Common:2; Rare:97 | ||||
| chr16:2474970-2475151 | Rare:56 | ||||
| chr16:2682350-2682608 | Rare:118 | ||||
| chr16:2777023-2777388 | Common:2; Rare:135 |