| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42781887-42782082 | Common:8; Rare:45 | ||||
| chr6:42879577-42879940 | Rare:106 | ||||
| chr6:42929106-42929277 | Common:2; Rare:47 | ||||
| chr6:42929381-42929594 | Common:1; Rare:79 | ||||
| chr6:42960617-42960777 | Common:1; Rare:38 | ||||
| chr6:42984284-42984629 | Rare:86 | ||||
| chr6:43006774-43007063 | Rare:62 | ||||
| chr6:43013784-43014329 | Common:2; Rare:139 | ||||
| chr6:43053771-43054246 | Common:5; Rare:138; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059793-43059890 | Rare:28 | ||||
| chr6:43060192-43060473 | Common:2; Rare:81 | ||||
| chr6:43171042-43171290 | Rare:61 | ||||
| chr6:43182105-43182233 | Rare:37 | ||||
| chr6:43229376-43229520 | Rare:57 | ||||
| chr6:43427443-43427599 | Rare:42 |