| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126211641-126211819 | Rare:82 | ||||
| chr11:126264247-126264477 | Rare:67 | ||||
| chr11:126264502-126264763 | Common:2; Rare:66 | ||||
| chr11:126268687-126269209 | Common:2; Rare:200; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126283002-126283136 | Common:1; Rare:51 | ||||
| chr11:126355542-126355771 | Common:1; Rare:62 | ||||
| chr11:128522269-128522551 | Common:1; Rare:91 | ||||
| chr11:129895529-129895687 | Common:2; Rare:62 | ||||
| chr11:130002774-130002951 | Common:2; Rare:34 | ||||
| chr11:130069593-130070079 | Common:2; Rare:179 | ||||
| chr11:130314395-130314497 | Common:1; Rare:31 | ||||
| chr11:130916265-130916396 | Common:1; Rare:24 | ||||
| chr11:134224533-134224695 | Rare:61 | ||||
| chr11:134225448-134225663 | Rare:63 | ||||
| chr11:134253292-134253602 | Common:2; Rare:110; Clinvar (benign):1 |