| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343538-127343639 | Common:1; Rare:29 | ||||
| chr6:128520561-128520787 | Common:1; Rare:84 | ||||
| chr6:129491074-129491251 | Rare:39 | ||||
| chr6:132401435-132401574 | Common:1; Rare:40 | ||||
| chr6:133952976-133953246 | Common:2; Rare:75 | ||||
| chr6:134174847-134175059 | Common:1; Rare:102 | ||||
| chr6:135497618-135497792 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289767-136290040 | Common:1; Rare:119 | ||||
| chr6:138404167-138404540 | Common:6; Rare:108 | ||||
| chr6:138773669-138773813 | Common:3; Rare:70 | ||||
| chr6:139028616-139028858 | Common:1; Rare:52 | ||||
| chr6:142147163-142147289 | Rare:51 | ||||
| chr6:142301844-142302110 | Common:6; Rare:72 | ||||
| chr6:143060742-143060922 | Common:7; Rare:62 | ||||
| chr6:143450654-143450929 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 |