| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:740984-741144 | Rare:52 | ||||
| chr16:970851-971192 | Common:7; Rare:156 | ||||
| chr16:1211484-1211748 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):5 | ||||
| chr16:1420703-1420937 | Common:1; Rare:97 | ||||
| chr16:1612032-1612369 | Common:2; Rare:116; Clinvar:1 | ||||
| chr16:1706069-1706384 | Common:3; Rare:97 | ||||
| chr16:1771511-1771623 | Rare:47 | ||||
| chr16:1773126-1773207 | Rare:19 | ||||
| chr16:1782508-1783009 | Common:4; Rare:166 | ||||
| chr16:1826770-1826982 | Common:3; Rare:68 | ||||
| chr16:1827135-1827538 | Common:3; Rare:203 | ||||
| chr16:1943183-1943470 | Rare:90 | ||||
| chr16:1964467-1964968 | Common:17; Rare:214 | ||||
| chr16:1971885-1972120 | Common:3; Rare:68 | ||||
| chr16:2047810-2048038 | Rare:103; Clinvar:2; Clinvar (benign):1 |