| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125592448-125592921 | Common:6; Rare:161 | ||||
| chr11:125614159-125614426 | Rare:59; Clinvar (benign):1 | ||||
| chr11:125625869-125626007 | Rare:44 | ||||
| chr11:125887459-125887743 | Common:2; Rare:90 | ||||
| chr11:126211595-126211822 | Rare:108 | ||||
| chr11:126266233-126266632 | Rare:132 | ||||
| chr11:126268463-126268661 | Common:3; Rare:51 | ||||
| chr11:126268760-126269215 | Common:2; Rare:179; Clinvar:3; Clinvar (benign):4 | ||||
| chr11:126270252-126270510 | Common:4; Rare:30 | ||||
| chr11:126303971-126304086 | Rare:65 | ||||
| chr11:126355540-126355742 | Common:1; Rare:49 | ||||
| chr11:127000231-127000318 | Rare:21 | ||||
| chr11:128522239-128522596 | Common:3; Rare:110 | ||||
| chr11:128522651-128522972 | Rare:68 | ||||
| chr11:128693882-128694265 | Rare:73 |