| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387434-20387771 | Common:7; Rare:109 | ||||
| chr11:27506739-27506868 | Common:1; Rare:55 | ||||
| chr11:28108115-28108396 | Common:1; Rare:84 | ||||
| chr11:30322971-30323154 | Common:1; Rare:53 | ||||
| chr11:31509561-31509784 | Common:1; Rare:70 | ||||
| chr11:32829656-32829957 | Common:4; Rare:63 | ||||
| chr11:33015762-33015908 | Common:1; Rare:54 | ||||
| chr11:33161456-33161657 | Common:6; Rare:54 | ||||
| chr11:33736404-33736612 | Common:1; Rare:68 | ||||
| chr11:34620830-34621155 | Common:2; Rare:72 | ||||
| chr11:34916301-34916667 | Common:10; Rare:149; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139012-35139181 | Common:1; Rare:38 | ||||
| chr11:36510249-36510370 | Rare:32 | ||||
| chr11:43358845-43359004 | Rare:77 | ||||
| chr11:46617248-46617585 | Common:5; Rare:94 |