| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133240546-133240844 | Rare:60 | ||||
| chr6:133240853-133240898 | Rare:8 | ||||
| chr6:133240961-133241663 | Common:8; Rare:189; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:133953049-133953269 | Common:2; Rare:73 | ||||
| chr6:134174850-134175029 | Common:1; Rare:85 | ||||
| chr6:135054778-135055007 | Common:6; Rare:68 | ||||
| chr6:135497581-135497880 | Common:4; Rare:110; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136289747-136290014 | Common:1; Rare:116 | ||||
| chr6:137219129-137219209 | Common:1; Rare:24 | ||||
| chr6:137219274-137219508 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:138773646-138773813 | Common:3; Rare:77 | ||||
| chr6:142147144-142147300 | Rare:61 | ||||
| chr6:143060700-143060919 | Common:7; Rare:73 | ||||
| chr6:143450667-143450999 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843136-143843431 | Common:2; Rare:98 |