| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75265804-75266204 | Common:22; Rare:415 | ||||
| chr16:75305379-75305919 | Common:3; Rare:171 | ||||
| chr16:75432863-75433273 | Common:14; Rare:247 | ||||
| chr16:75433308-75433910 | Common:35; Rare:1183 | ||||
| chr16:75433914-75434192 | Rare:128 | ||||
| chr16:75464210-75465071 | Common:30; Rare:954 | ||||
| chr16:75555105-75556062 | Common:38; Rare:859; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr16:75556033-75556198 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:75556126-75556526 | Common:13; Rare:549; Clinvar:1; Clinvar (benign):27; Clinvar (pathogenic):3 | ||||
| chr16:75556552-75556952 | Common:1; Rare:84 | ||||
| chr16:75566131-75566531 | Common:10; Rare:577 | ||||
| chr16:75566601-75567314 | Common:4; Rare:386 | ||||
| chr16:75622490-75622970 | Common:2; Rare:109 | ||||
| chr16:75622990-75623140 | Common:6; Rare:49 | ||||
| chr16:75623160-75623890 | Common:23; Rare:561 |