| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:123502098-123502411 | Common:2; Rare:55 | ||||
| chr6:123502662-123502833 | Common:2; Rare:26 | ||||
| chr6:123509784-123510084 | Common:1; Rare:60 | ||||
| chr6:123519228-123519426 | Common:1; Rare:32 | ||||
| chr6:129512269-129512493 | Rare:68; Clinvar:5; Clinvar (benign):3 | ||||
| chr6:134343190-134343334 | Common:2; Rare:28 | ||||
| chr6:136072808-136073114 | Common:3; Rare:42 | ||||
| chr6:137218046-137218099 | Rare:10 | ||||
| chr6:138570746-138570894 | Rare:28 | ||||
| chr6:138833885-138834190 | Common:1; Rare:41 | ||||
| chr6:139250589-139250822 | Rare:34 | ||||
| chr6:139289362-139289418 | Rare:11 | ||||
| chr6:140079365-140079532 | Rare:22 | ||||
| chr6:140639008-140639284 | Common:1; Rare:49 | ||||
| chr6:141403255-141403511 | Common:3; Rare:54 |