| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118651591-118651754 | Common:4; Rare:52 | ||||
| chr6:118893908-118894236 | Common:2; Rare:98 | ||||
| chr6:122471768-122471921 | Common:2; Rare:45 | ||||
| chr6:125790874-125790968 | Common:2; Rare:29 | ||||
| chr6:125986385-125986548 | Rare:54 | ||||
| chr6:127343349-127343619 | Common:2; Rare:60 | ||||
| chr6:128520561-128520791 | Common:1; Rare:85 | ||||
| chr6:136289767-136290020 | Common:1; Rare:109 | ||||
| chr6:136550400-136550717 | Common:2; Rare:90 | ||||
| chr6:137219350-137219548 | Common:4; Rare:71; Clinvar (benign):2 | ||||
| chr6:138773655-138773802 | Common:3; Rare:67 | ||||
| chr6:142301774-142302077 | Common:6; Rare:83 | ||||
| chr6:142302271-142302675 | Common:1; Rare:97 | ||||
| chr6:143060700-143060919 | Common:7; Rare:73 | ||||
| chr6:143450660-143450929 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 |