| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1782508-1783023 | Common:4; Rare:172 | ||||
| chr16:1826536-1827000 | Common:7; Rare:143 | ||||
| chr16:1827171-1827532 | Common:3; Rare:188 | ||||
| chr16:1943125-1943530 | Common:1; Rare:129 | ||||
| chr16:1964761-1965061 | Common:14; Rare:140 | ||||
| chr16:1971888-1972110 | Common:2; Rare:64 | ||||
| chr16:2009678-2009920 | Common:15; Rare:104 | ||||
| chr16:2035566-2035979 | Common:4; Rare:137 | ||||
| chr16:2047242-2047432 | Rare:46 | ||||
| chr16:2047769-2048058 | Rare:144; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:2155344-2155508 | Rare:50 | ||||
| chr16:2155519-2155828 | Common:2; Rare:91 | ||||
| chr16:2268071-2268172 | Rare:47 | ||||
| chr16:2268355-2268482 | Common:1; Rare:42 | ||||
| chr16:2429112-2429484 | Common:3; Rare:121 |