| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:117602451-117602641 | Common:3; Rare:56 | ||||
| chr6:118893885-118894234 | Common:3; Rare:105 | ||||
| chr6:122471768-122471921 | Common:2; Rare:45 | ||||
| chr6:125986330-125986548 | Common:1; Rare:75 | ||||
| chr6:127343348-127343603 | Common:1; Rare:55 | ||||
| chr6:128520571-128520747 | Rare:68 | ||||
| chr6:132401428-132401602 | Common:1; Rare:52 | ||||
| chr6:136289779-136290041 | Common:2; Rare:114 | ||||
| chr6:137219350-137219527 | Common:4; Rare:60; Clinvar (benign):2 | ||||
| chr6:142147120-142147285 | Common:3; Rare:58 | ||||
| chr6:143060711-143060919 | Common:7; Rare:70 | ||||
| chr6:143450667-143450929 | Common:1; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843152-143843391 | Common:2; Rare:75 | ||||
| chr6:149648624-149648843 | Common:1; Rare:66 | ||||
| chr6:149749482-149749796 | Rare:132 |