| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65920662-65920970 | Common:1; Rare:105 | ||||
| chr11:65921120-65921450 | Common:1; Rare:106 | ||||
| chr11:65976560-65976638 | Rare:31 | ||||
| chr11:66002105-66002410 | Common:3; Rare:89; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:66002453-66002521 | Rare:16; Clinvar:1 | ||||
| chr11:66021134-66021255 | Rare:34 | ||||
| chr11:66288996-66289389 | Common:1; Rare:99 | ||||
| chr11:66316512-66316703 | Rare:64 | ||||
| chr11:66480226-66480444 | Common:1; Rare:58 | ||||
| chr11:66593050-66593232 | Common:1; Rare:65 | ||||
| chr11:66616422-66616653 | Common:1; Rare:62 | ||||
| chr11:66843334-66843456 | Common:5; Rare:62 | ||||
| chr11:67508637-67508772 | Common:3; Rare:51 | ||||
| chr11:68030616-68030768 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271900-68272106 | Common:2; Rare:87 |