| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1782508-1782878 | Common:4; Rare:120 | ||||
| chr16:1827157-1827232 | Common:1; Rare:33 | ||||
| chr16:1943189-1943499 | Common:1; Rare:93 | ||||
| chr16:1957749-1957918 | Common:3; Rare:53 | ||||
| chr16:1963107-1963376 | Common:4; Rare:87 | ||||
| chr16:1964572-1964944 | Common:14; Rare:164 | ||||
| chr16:1971888-1972113 | Common:2; Rare:66 | ||||
| chr16:2033125-2033304 | Rare:44 | ||||
| chr16:2047770-2048033 | Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2223518-2223671 | Rare:70 | ||||
| chr16:2268072-2268225 | Common:1; Rare:62 | ||||
| chr16:2459980-2460118 | Rare:36 | ||||
| chr16:2514071-2514178 | Common:1; Rare:35 | ||||
| chr16:2520196-2520406 | Common:8; Rare:128 | ||||
| chr16:2682388-2682598 | Rare:95 |