| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133241257-133241466 | Common:4; Rare:90; Clinvar:1 | ||||
| chr6:133953031-133953290 | Common:4; Rare:156 | ||||
| chr6:134174831-134175128 | Common:2; Rare:255 | ||||
| chr6:135054752-135055034 | Common:12; Rare:153 | ||||
| chr6:135497569-135497916 | Common:8; Rare:205; Clinvar:3; Clinvar (benign):4 | ||||
| chr6:136250254-136250570 | Common:4; Rare:177 | ||||
| chr6:136289200-136289460 | Rare:98 | ||||
| chr6:136289743-136290065 | Common:4; Rare:271 | ||||
| chr6:137219109-137219469 | Common:8; Rare:262; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr6:137866909-137867495 | Rare:235 | ||||
| chr6:138107298-138107584 | Common:4; Rare:124 | ||||
| chr6:138161867-138162012 | Common:8; Rare:94 | ||||
| chr6:138404057-138404545 | Common:12; Rare:259 | ||||
| chr6:138499323-138499630 | Common:4; Rare:110 | ||||
| chr6:138545497-138546350 | Common:8; Rare:194 |