| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47185360-47185498 | Common:2; Rare:37 | ||||
| chr11:47186347-47186489 | Rare:45 | ||||
| chr11:47214814-47215110 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248774-47248957 | Rare:75 | ||||
| chr11:47257506-47257749 | Common:1; Rare:35 | ||||
| chr11:47269492-47269778 | Common:1; Rare:91 | ||||
| chr11:47269974-47270212 | Common:1; Rare:84 | ||||
| chr11:47378379-47378653 | Rare:71 | ||||
| chr11:47426412-47426648 | Rare:57 | ||||
| chr11:47565460-47565650 | Common:3; Rare:38 | ||||
| chr11:47578931-47579128 | Rare:108; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642434-47642805 | Rare:134 | ||||
| chr11:47767164-47767460 | Common:2; Rare:126 | ||||
| chr11:47848298-47848398 | Common:1; Rare:53 | ||||
| chr11:47848540-47848629 | Common:1; Rare:15 |