| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75116726-75116887 | Common:2; Rare:39 | ||||
| chr16:75433288-75433959 | Common:5; Rare:225 | ||||
| chr16:75433982-75434087 | Rare:19 | ||||
| chr16:75555266-75555420 | Common:1; Rare:35 | ||||
| chr16:75556183-75556378 | Common:3; Rare:72; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr16:75566232-75566519 | Common:2; Rare:142 | ||||
| chr16:75623222-75623437 | Common:3; Rare:78 | ||||
| chr16:75647614-75647866 | Common:4; Rare:129; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648068-75648611 | Rare:208 | ||||
| chr16:75648614-75648667 | Rare:23 | ||||
| chr16:76277188-76277604 | Common:2; Rare:86 | ||||
| chr16:77190683-77191221 | Common:13; Rare:184 | ||||
| chr16:79600730-79600958 | Common:1; Rare:65 | ||||
| chr16:80540894-80541067 | Common:3; Rare:73 | ||||
| chr16:81006791-81007272 | Common:5; Rare:161 |