| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30717171-30717466 | Common:1; Rare:70 | ||||
| chr6:30720252-30720480 | Common:1; Rare:66 | ||||
| chr6:30721323-30721654 | Common:2; Rare:144 | ||||
| chr6:30742481-30742968 | Common:3; Rare:114 | ||||
| chr6:30907964-30908240 | Common:2; Rare:62 | ||||
| chr6:30913942-30914363 | Common:2; Rare:132; Clinvar (benign):2 | ||||
| chr6:30955632-30955865 | Common:3; Rare:48 | ||||
| chr6:31158063-31158557 | Common:8; Rare:116 | ||||
| chr6:31272024-31272247 | Common:14; Rare:48 | ||||
| chr6:31356905-31357250 | Common:41; Rare:104 | ||||
| chr6:31399729-31400079 | Common:7; Rare:61 | ||||
| chr6:31541573-31541593 | Common:1; Rare:10 | ||||
| chr6:31541741-31541777 | Rare:8 | ||||
| chr6:31541909-31542406 | Common:9; Rare:139 | ||||
| chr6:31546557-31546887 | Common:3; Rare:66 |