| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126283013-126283131 | Common:1; Rare:47 | ||||
| chr11:126355531-126355738 | Common:1; Rare:55 | ||||
| chr11:128522263-128522596 | Common:3; Rare:105 | ||||
| chr11:128692800-128692978 | Rare:45 | ||||
| chr11:129279490-129279746 | Common:3; Rare:112 | ||||
| chr11:130069624-130070079 | Common:2; Rare:161 | ||||
| chr11:130314403-130314528 | Common:1; Rare:43 | ||||
| chr11:130448401-130448710 | Common:1; Rare:72 | ||||
| chr11:134223919-134224166 | Common:2; Rare:80 | ||||
| chr11:134224525-134224695 | Rare:64 | ||||
| chr11:134253290-134253606 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:389230-389364 | Rare:49 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:610367-610444 | Rare:9 | ||||
| chr12:643616-643668 | Rare:9 |