| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132814449-132814777 | Common:5; Rare:167 | ||||
| chr6:133952974-133953306 | Common:2; Rare:97 | ||||
| chr6:134174855-134174972 | Rare:46 | ||||
| chr6:134317779-134318041 | Common:1; Rare:55 | ||||
| chr6:135054784-135054990 | Common:6; Rare:62 | ||||
| chr6:135497612-135497834 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289752-136290024 | Common:1; Rare:118 | ||||
| chr6:136550372-136550696 | Common:2; Rare:98 | ||||
| chr6:137219254-137219463 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:138404175-138404569 | Common:7; Rare:108 | ||||
| chr6:138512486-138512725 | Rare:32 | ||||
| chr6:138572523-138572723 | Common:1; Rare:44 | ||||
| chr6:138773379-138773547 | Common:2; Rare:89 | ||||
| chr6:138773657-138773827 | Common:3; Rare:83 | ||||
| chr6:139028172-139028538 | Common:1; Rare:57 |