| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:981263-981444 | Common:16; Rare:109 | ||||
| chr16:1309389-1309731 | Rare:129 | ||||
| chr16:1414697-1414919 | Common:5; Rare:56 | ||||
| chr16:1420712-1420918 | Common:1; Rare:84 | ||||
| chr16:1493263-1493572 | Common:4; Rare:97 | ||||
| chr16:1533486-1533688 | Common:1; Rare:40 | ||||
| chr16:1612040-1612360 | Common:2; Rare:106; Clinvar:1 | ||||
| chr16:1706047-1706286 | Common:2; Rare:70 | ||||
| chr16:1771499-1771868 | Common:3; Rare:146 | ||||
| chr16:1782508-1783009 | Common:4; Rare:166 | ||||
| chr16:1943197-1943497 | Common:1; Rare:87 | ||||
| chr16:1959424-1959658 | Common:5; Rare:104 | ||||
| chr16:1964823-1964944 | Common:4; Rare:43 | ||||
| chr16:1971935-1972123 | Common:1; Rare:55 | ||||
| chr16:2047784-2048043 | Rare:120; Clinvar:2; Clinvar (benign):1 |