| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133953058-133953277 | Common:2; Rare:75 | ||||
| chr6:134174852-134175032 | Common:1; Rare:85 | ||||
| chr6:135054784-135055031 | Common:6; Rare:74 | ||||
| chr6:135497618-135497834 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289774-136290014 | Common:1; Rare:104 | ||||
| chr6:138773689-138773802 | Common:3; Rare:54 | ||||
| chr6:142147191-142147284 | Rare:35 | ||||
| chr6:142301636-142302119 | Common:9; Rare:131 | ||||
| chr6:143060724-143060935 | Common:7; Rare:76 | ||||
| chr6:143450654-143450956 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511435-143511614 | Rare:60 | ||||
| chr6:143511651-143511774 | Common:4; Rare:32 | ||||
| chr6:145814664-145814915 | Common:1; Rare:112 | ||||
| chr6:145964330-145964596 | Rare:90 | ||||
| chr6:151325409-151325699 | Common:2; Rare:66 |