| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132798617-132798662 | Common:2; Rare:9 | ||||
| chr6:132814276-132814607 | Common:3; Rare:118 | ||||
| chr6:133952951-133953304 | Common:2; Rare:102 | ||||
| chr6:135497621-135497886 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:135851581-135851780 | Rare:36 | ||||
| chr6:135852064-135852133 | Rare:8 | ||||
| chr6:136289773-136290077 | Common:2; Rare:134 | ||||
| chr6:138773651-138773802 | Common:3; Rare:69 | ||||
| chr6:139028604-139028857 | Common:1; Rare:54 | ||||
| chr6:143060750-143060908 | Common:6; Rare:57 | ||||
| chr6:143450660-143450956 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511678-143511990 | Common:5; Rare:59 | ||||
| chr6:143843179-143843393 | Common:2; Rare:67 | ||||
| chr6:144064565-144064690 | Common:2; Rare:27 | ||||
| chr6:144343830-144344217 | Common:4; Rare:68 |