| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1612032-1612372 | Common:2; Rare:118; Clinvar:1 | ||||
| chr16:1706026-1706408 | Common:5; Rare:126 | ||||
| chr16:1771505-1771868 | Common:3; Rare:143 | ||||
| chr16:1773126-1773185 | Rare:12 | ||||
| chr16:1782510-1783018 | Common:4; Rare:169 | ||||
| chr16:1826761-1826975 | Common:3; Rare:72 | ||||
| chr16:1827179-1827574 | Common:3; Rare:205 | ||||
| chr16:1943163-1943529 | Common:1; Rare:115 | ||||
| chr16:1959431-1959666 | Common:5; Rare:105 | ||||
| chr16:1964802-1965074 | Common:7; Rare:123 | ||||
| chr16:1971878-1972117 | Common:3; Rare:71 | ||||
| chr16:2009650-2009983 | Common:16; Rare:140 | ||||
| chr16:2047770-2048050 | Rare:136; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:2155663-2155815 | Common:1; Rare:44 | ||||
| chr16:2205683-2205921 | Common:4; Rare:112 |