| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74984307-74984624 | Common:1; Rare:82 | ||||
| chr16:74985024-74985383 | Common:3; Rare:115 | ||||
| chr16:74998705-74999130 | Common:4; Rare:159 | ||||
| chr16:75148361-75148606 | Common:4; Rare:109 | ||||
| chr16:75148716-75149087 | Common:3; Rare:161 | ||||
| chr16:75250869-75251067 | Common:2; Rare:62 | ||||
| chr16:75251609-75251835 | Common:1; Rare:84 | ||||
| chr16:75265900-75266158 | Common:6; Rare:104 | ||||
| chr16:75433182-75433302 | Rare:52 | ||||
| chr16:75433352-75433879 | Common:4; Rare:174 | ||||
| chr16:75464250-75464554 | Common:5; Rare:141 | ||||
| chr16:75464600-75464846 | Common:1; Rare:93 | ||||
| chr16:75495388-75495595 | Common:2; Rare:79 | ||||
| chr16:75555257-75555449 | Common:3; Rare:43 | ||||
| chr16:75555910-75556455 | Common:4; Rare:209; Clinvar:2; Clinvar (benign):11; Clinvar (pathogenic):2 |