| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:132401428-132401632 | Common:2; Rare:61 | ||||
| chr6:132513006-132513230 | Common:1; Rare:55 | ||||
| chr6:132814255-132814611 | Common:4; Rare:129 | ||||
| chr6:133240724-133240781 | Rare:11 | ||||
| chr6:133241022-133241438 | Common:5; Rare:124 | ||||
| chr6:133888981-133889209 | Common:1; Rare:37 | ||||
| chr6:133889316-133889417 | Common:2; Rare:32 | ||||
| chr6:133952367-133952495 | Rare:23 | ||||
| chr6:133953031-133953280 | Common:2; Rare:79 | ||||
| chr6:134174803-134175029 | Common:1; Rare:125 | ||||
| chr6:135054763-135054925 | Common:5; Rare:51 | ||||
| chr6:135497604-135497873 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136038293-136038446 | Common:1; Rare:39 | ||||
| chr6:136289774-136290042 | Common:2; Rare:116 | ||||
| chr6:137219075-137219197 | Rare:29 |