| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343334-127343429 | Rare:19 | ||||
| chr6:127343459-127343639 | Common:2; Rare:48 | ||||
| chr6:136289779-136290068 | Common:2; Rare:129 | ||||
| chr6:138773650-138773814 | Common:3; Rare:77 | ||||
| chr6:143450656-143450927 | Common:1; Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:144285125-144285342 | Common:2; Rare:70 | ||||
| chr6:151391543-151391862 | Common:3; Rare:85 | ||||
| chr6:151452034-151452538 | Common:4; Rare:176 | ||||
| chr6:153002666-153002841 | Common:3; Rare:58 | ||||
| chr6:154510542-154510875 | Common:3; Rare:101 | ||||
| chr6:158168254-158168392 | Common:2; Rare:51 | ||||
| chr6:159727039-159727153 | Rare:36 | ||||
| chr6:159727309-159727679 | Common:6; Rare:146 | ||||
| chr6:159762310-159762564 | Common:2; Rare:67 | ||||
| chr6:159789452-159789466 | Rare:6 |