| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1612037-1612335 | Common:1; Rare:97; Clinvar:1 | ||||
| chr16:1706031-1706391 | Common:4; Rare:117 | ||||
| chr16:1773126-1773390 | Rare:99 | ||||
| chr16:1826765-1826975 | Common:3; Rare:70 | ||||
| chr16:1827137-1827521 | Common:3; Rare:193 | ||||
| chr16:1943149-1943515 | Common:1; Rare:118 | ||||
| chr16:1959485-1959752 | Common:4; Rare:124 | ||||
| chr16:1964499-1964996 | Common:17; Rare:216 | ||||
| chr16:1971915-1972090 | Common:1; Rare:50 | ||||
| chr16:2047804-2048058 | Rare:127; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:2268063-2268186 | Common:1; Rare:61 | ||||
| chr16:2340754-2341071 | Common:2; Rare:110 | ||||
| chr16:2474983-2475151 | Rare:53 | ||||
| chr16:2513650-2514178 | Common:1; Rare:201 | ||||
| chr16:2752603-2752851 | Common:2; Rare:112 |