| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133953064-133953255 | Common:2; Rare:64 | ||||
| chr6:134174849-134174992 | Common:1; Rare:63 | ||||
| chr6:135497603-135497902 | Common:4; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289747-136290054 | Common:2; Rare:133 | ||||
| chr6:137219316-137219527 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:137866931-137867369 | Rare:100 | ||||
| chr6:138106809-138107093 | Common:6; Rare:55 | ||||
| chr6:138773476-138773865 | Common:5; Rare:192 | ||||
| chr6:139028729-139028826 | Common:1; Rare:17 | ||||
| chr6:139374498-139374935 | Common:1; Rare:174 | ||||
| chr6:142147116-142147290 | Common:3; Rare:62 | ||||
| chr6:143060724-143060928 | Common:7; Rare:72 | ||||
| chr6:143450654-143450956 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843206-143843402 | Common:2; Rare:63 | ||||
| chr6:144285256-144285510 | Common:2; Rare:57 |