| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166955830-166956277 | Common:6; Rare:203; Clinvar:6; Clinvar (benign):4 | ||||
| chr6:166956460-166956807 | Common:14; Rare:202; Clinvar:6; Clinvar (benign):4 | ||||
| chr6:166957144-166957630 | Common:7; Rare:153 | ||||
| chr6:166998997-166999437 | Common:4; Rare:286 | ||||
| chr6:166999834-166999952 | Rare:35 | ||||
| chr6:167122900-167123195 | Rare:87 | ||||
| chr6:167291009-167291397 | Common:3; Rare:60 | ||||
| chr6:167826381-167826630 | Common:10; Rare:118 | ||||
| chr6:167826699-167827002 | Common:4; Rare:317 | ||||
| chr6:167827190-167827677 | Common:9; Rare:222 | ||||
| chr6:167827870-167828120 | Rare:112 | ||||
| chr6:169701921-169702366 | Common:11; Rare:334 | ||||
| chr6:169723905-169724113 | Common:3; Rare:94 | ||||
| chr6:169724423-169724843 | Rare:207 | ||||
| chr6:169725200-169725700 | Common:4; Rare:172 |