| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85647875-85647998 | Rare:28; Clinvar:2 | ||||
| chr11:85665047-85665293 | Common:1; Rare:84 | ||||
| chr11:86244437-86244848 | Common:1; Rare:111 | ||||
| chr11:88337703-88337888 | Common:3; Rare:86; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:90223008-90223195 | Common:1; Rare:75 | ||||
| chr11:93661456-93661745 | Common:1; Rare:80 | ||||
| chr11:93741329-93741702 | Common:8; Rare:146 | ||||
| chr11:93784182-93784362 | Common:3; Rare:57 | ||||
| chr11:94493780-94494018 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973539-94973719 | Rare:52 | ||||
| chr11:95089712-95089872 | Common:3; Rare:65 | ||||
| chr11:95231412-95231590 | Common:1; Rare:45 | ||||
| chr11:95790369-95790590 | Common:1; Rare:82 | ||||
| chr11:96389851-96390043 | Common:1; Rare:80 | ||||
| chr11:102317165-102317580 | Rare:71 |