| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31357088-31357384 | Common:29; Rare:54 | ||||
| chr6:31547423-31547644 | Common:2; Rare:43 | ||||
| chr6:31620360-31620787 | Common:1; Rare:132 | ||||
| chr6:31644095-31644381 | Rare:93 | ||||
| chr6:31664922-31665282 | Common:3; Rare:90 | ||||
| chr6:31665859-31666207 | Common:4; Rare:96 | ||||
| chr6:31703285-31703425 | Rare:46 | ||||
| chr6:31729300-31729441 | Rare:21 | ||||
| chr6:31736410-31736599 | Common:1; Rare:39 | ||||
| chr6:31815360-31815663 | Common:3; Rare:115 | ||||
| chr6:31897679-31897782 | Rare:20 | ||||
| chr6:31950099-31950397 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:31958860-31959198 | Rare:112; Clinvar:8 | ||||
| chr6:32109275-32109578 | Rare:45 | ||||
| chr6:32153222-32153549 | Rare:50 |