| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31665867-31666149 | Common:3; Rare:80 | ||||
| chr6:31736285-31736599 | Common:2; Rare:74 | ||||
| chr6:31815350-31815544 | Common:1; Rare:61 | ||||
| chr6:31958863-31959191 | Rare:107; Clinvar:8 | ||||
| chr6:32844002-32844086 | Rare:22; Clinvar:1 | ||||
| chr6:32853690-32853814 | Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:32854010-32854209 | Common:2; Rare:49 | ||||
| chr6:33200656-33200966 | Common:3; Rare:92 | ||||
| chr6:33271842-33272122 | Common:1; Rare:117 | ||||
| chr6:33289523-33289633 | Rare:26 | ||||
| chr6:33298908-33299064 | Rare:41 | ||||
| chr6:33417879-33417948 | Rare:29 | ||||
| chr6:33418048-33418495 | Common:3; Rare:107 | ||||
| chr6:33580243-33580364 | Common:2; Rare:30 | ||||
| chr6:34236752-34236906 | Common:2; Rare:63 |