| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1309340-1309735 | Rare:144 | ||||
| chr16:1351717-1352011 | Common:2; Rare:137; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1379143-1379239 | Rare:31 | ||||
| chr16:1379460-1379802 | Common:2; Rare:131 | ||||
| chr16:1413995-1414120 | Common:2; Rare:40 | ||||
| chr16:1414595-1414924 | Common:6; Rare:102 | ||||
| chr16:1420651-1421382 | Common:10; Rare:232 | ||||
| chr16:1459074-1459295 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:1474983-1475243 | Common:5; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:1475484-1475518 | Common:1; Rare:7 | ||||
| chr16:1493153-1493512 | Common:4; Rare:115 | ||||
| chr16:1533483-1533706 | Common:1; Rare:43 | ||||
| chr16:1610648-1610903 | Common:1; Rare:81; Clinvar:1 | ||||
| chr16:1611937-1612511 | Common:6; Rare:214; Clinvar:2 | ||||
| chr16:1677938-1678490 | Common:3; Rare:181 |