| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67845550-67845964 | Common:2; Rare:172 | ||||
| chr16:67874193-67874593 | Common:2; Rare:120 | ||||
| chr16:67940102-67940788 | Common:2; Rare:209; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr16:67947916-67949070 | Common:3; Rare:295 | ||||
| chr16:67975587-67976013 | Common:3; Rare:173 | ||||
| chr16:67983041-67984118 | Common:9; Rare:378 | ||||
| chr16:67984849-67985014 | Rare:27 | ||||
| chr16:67989650-67990140 | Common:8; Rare:163 | ||||
| chr16:67992527-67993050 | Common:5; Rare:186 | ||||
| chr16:68005918-68006318 | Common:2; Rare:73 | ||||
| chr16:68070950-68071350 | Common:1; Rare:138 | ||||
| chr16:68074820-68075280 | Common:2; Rare:145 | ||||
| chr16:68079576-68079976 | Common:2; Rare:108 | ||||
| chr16:68080116-68080247 | Rare:24 | ||||
| chr16:68200147-68200547 | Rare:101 |