| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33322891-33323246 | Common:5; Rare:116 | ||||
| chr6:33391625-33391885 | Common:1; Rare:62 | ||||
| chr6:33410887-33411060 | Rare:34 | ||||
| chr6:33417254-33417511 | Rare:74 | ||||
| chr6:33417618-33418558 | Common:4; Rare:254 | ||||
| chr6:33419952-33420307 | Rare:71; Clinvar (benign):1 | ||||
| chr6:33454422-33454604 | Rare:46 | ||||
| chr6:33580171-33580376 | Common:2; Rare:56 | ||||
| chr6:33711638-33711811 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr6:33789118-33789247 | Common:1; Rare:64 | ||||
| chr6:34236755-34236914 | Common:2; Rare:63 | ||||
| chr6:34248449-34248581 | Rare:22 | ||||
| chr6:34248977-34249274 | Common:1; Rare:70 | ||||
| chr6:34391954-34392887 | Common:4; Rare:323 | ||||
| chr6:34425968-34426188 | Common:5; Rare:90; Clinvar:1; Clinvar (benign):8 |