| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67469229-67469439 | Common:1; Rare:59 | ||||
| chr11:67482906-67483161 | Rare:57; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68030381-68030733 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271926-68272134 | Common:2; Rare:92 | ||||
| chr11:68903795-68903943 | Common:4; Rare:67; Clinvar (benign):6 | ||||
| chr11:69675300-69675472 | Rare:47 | ||||
| chr11:70203144-70203330 | Common:3; Rare:70 | ||||
| chr11:70398335-70398596 | Common:2; Rare:87 | ||||
| chr11:70826694-70826748 | Rare:6 | ||||
| chr11:71448344-71448690 | Common:4; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928457-71928729 | Rare:70 | ||||
| chr11:71928930-71929082 | Common:1; Rare:50 | ||||
| chr11:72041056-72041223 | Common:1; Rare:25 | ||||
| chr11:72041857-72041904 | Common:1; Rare:9 | ||||
| chr11:72041949-72042059 | Rare:25 |