| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125625864-125626012 | Rare:48 | ||||
| chr11:125903159-125903333 | Rare:42 | ||||
| chr11:125904205-125904515 | Common:1; Rare:91 | ||||
| chr11:126211623-126211812 | Rare:87 | ||||
| chr11:126268775-126269209 | Common:2; Rare:168; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126283024-126283131 | Rare:43 | ||||
| chr11:126303931-126304083 | Rare:80 | ||||
| chr11:126355526-126355752 | Common:2; Rare:60 | ||||
| chr11:129279489-129279765 | Common:4; Rare:120 | ||||
| chr11:129895516-129895677 | Common:2; Rare:65 | ||||
| chr11:130069552-130069940 | Common:2; Rare:147 | ||||
| chr11:130314418-130314495 | Common:1; Rare:21 | ||||
| chr11:130916405-130916669 | Common:6; Rare:81 | ||||
| chr11:134068891-134069086 | Rare:92; Clinvar (pathogenic):1 | ||||
| chr11:134223911-134224103 | Common:2; Rare:61 |