| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30492376-30492583 | Common:2; Rare:69 | ||||
| chr6:30516134-30516275 | Common:3; Rare:33 | ||||
| chr6:30602552-30602869 | Common:2; Rare:81 | ||||
| chr6:31119418-31119621 | Common:8; Rare:25 | ||||
| chr6:31186053-31186246 | Common:6; Rare:38 | ||||
| chr6:31400604-31400721 | Common:4; Rare:26 | ||||
| chr6:31719593-31719757 | Common:1; Rare:31 | ||||
| chr6:31720091-31720522 | Common:2; Rare:85 | ||||
| chr6:31720702-31720971 | Common:1; Rare:27 | ||||
| chr6:32188137-32188281 | Common:1; Rare:34 | ||||
| chr6:32853037-32853211 | Rare:46; Clinvar (benign):3 | ||||
| chr6:32894554-32894803 | Common:9; Rare:68 | ||||
| chr6:33249379-33249568 | Rare:57 | ||||
| chr6:33633610-33633875 | Common:5; Rare:77 | ||||
| chr6:33657962-33658147 | Rare:41 |