| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343314-127343429 | Rare:26 | ||||
| chr6:127343526-127343840 | Common:1; Rare:62 | ||||
| chr6:131628080-131628461 | Common:3; Rare:100 | ||||
| chr6:132714046-132714139 | Rare:29 | ||||
| chr6:132814274-132814616 | Common:3; Rare:126 | ||||
| chr6:132814752-132815072 | Common:4; Rare:145 | ||||
| chr6:135054769-135055007 | Common:6; Rare:72 | ||||
| chr6:135497618-135497893 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289779-136290020 | Common:1; Rare:104 | ||||
| chr6:136526344-136526529 | Common:3; Rare:32 | ||||
| chr6:136526555-136526600 | Rare:8 | ||||
| chr6:136550414-136550495 | Rare:28 | ||||
| chr6:138773642-138773825 | Common:3; Rare:87 | ||||
| chr6:139028632-139028870 | Common:1; Rare:51 | ||||
| chr6:143450652-143450929 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 |