| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33200656-33200925 | Common:2; Rare:82 | ||||
| chr6:33208443-33208533 | Rare:23 | ||||
| chr6:33271836-33272122 | Common:1; Rare:118 | ||||
| chr6:33289308-33289661 | Common:3; Rare:73 | ||||
| chr6:33299362-33299495 | Common:1; Rare:26 | ||||
| chr6:33322962-33323265 | Common:4; Rare:83 | ||||
| chr6:33417879-33417952 | Rare:32 | ||||
| chr6:33418024-33418495 | Common:3; Rare:114 | ||||
| chr6:33420000-33420301 | Rare:60; Clinvar (benign):1 | ||||
| chr6:33454431-33454593 | Rare:42 | ||||
| chr6:33580237-33580364 | Common:2; Rare:32 | ||||
| chr6:34248984-34249282 | Common:1; Rare:74 | ||||
| chr6:34392343-34392643 | Rare:118 | ||||
| chr6:34425993-34426144 | Common:4; Rare:69; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34514675-34514909 | Common:2; Rare:55 |