| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:35157-35385 | Common:4; Rare:32 | ||||
| chr16:1331810-1332052 | Common:2; Rare:50 | ||||
| chr16:1350038-1350438 | Common:2; Rare:154 | ||||
| chr16:1713903-1714315 | Common:3; Rare:98 | ||||
| chr16:1961963-1962163 | Common:3; Rare:81 | ||||
| chr16:2510053-2510217 | Common:1; Rare:29 | ||||
| chr16:2515329-2515472 | Rare:42 | ||||
| chr16:2515910-2516225 | Rare:67 | ||||
| chr16:2603097-2603456 | Common:3; Rare:139 | ||||
| chr16:2756852-2756865 | Rare:4 | ||||
| chr16:4307510-4307913 | Common:3; Rare:139 | ||||
| chr16:8839840-8839997 | Common:6; Rare:29 | ||||
| chr16:9094779-9095040 | Common:1; Rare:72 | ||||
| chr16:10888702-10888857 | Common:3; Rare:40 | ||||
| chr16:10895464-10895764 | Common:4; Rare:84; Clinvar:4; Clinvar (benign):1 |