| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31546561-31546915 | Common:3; Rare:69 | ||||
| chr6:31547436-31547730 | Common:2; Rare:78 | ||||
| chr6:31651907-31652063 | Rare:35 | ||||
| chr6:31652146-31652480 | Common:9; Rare:89 | ||||
| chr6:31665601-31666165 | Common:7; Rare:144 | ||||
| chr6:31703297-31703445 | Rare:46 | ||||
| chr6:31736261-31736595 | Common:2; Rare:83 | ||||
| chr6:31815321-31815571 | Common:1; Rare:85 | ||||
| chr6:31897670-31897785 | Rare:22 | ||||
| chr6:31958840-31959182 | Rare:102; Clinvar:8 | ||||
| chr6:31966826-31967111 | Common:1; Rare:69; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr6:32130164-32130410 | Common:2; Rare:43 | ||||
| chr6:32151908-32151943 | Rare:13 | ||||
| chr6:32176019-32176251 | Common:1; Rare:49 | ||||
| chr6:32178074-32178447 | Common:3; Rare:55 |