| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31546579-31546870 | Common:3; Rare:56 | ||||
| chr6:31547447-31547724 | Common:2; Rare:74 | ||||
| chr6:31620414-31620787 | Common:1; Rare:121 | ||||
| chr6:31652621-31652799 | Common:2; Rare:32 | ||||
| chr6:31665832-31666140 | Common:3; Rare:84 | ||||
| chr6:31728710-31728994 | Rare:72 | ||||
| chr6:31736261-31736586 | Common:2; Rare:80 | ||||
| chr6:31815319-31815579 | Common:1; Rare:92 | ||||
| chr6:31827491-31827741 | Common:2; Rare:74 | ||||
| chr6:31958885-31959148 | Rare:83; Clinvar:6 | ||||
| chr6:32154352-32154487 | Rare:19 | ||||
| chr6:32176028-32176248 | Common:1; Rare:45 | ||||
| chr6:32178074-32178447 | Common:3; Rare:55 | ||||
| chr6:32843911-32844119 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32844305-32844839 | Common:1; Rare:117 |