| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66285456-66285753 | Common:1; Rare:96 | ||||
| chr11:66289072-66289398 | Common:1; Rare:77 | ||||
| chr11:66347587-66347763 | Common:1; Rare:41 | ||||
| chr11:66480253-66480446 | Common:1; Rare:49 | ||||
| chr11:66593042-66593220 | Common:1; Rare:65 | ||||
| chr11:67428324-67428529 | Rare:71 | ||||
| chr11:67443441-67443707 | Common:2; Rare:92 | ||||
| chr11:67482901-67483161 | Rare:59; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67612088-67612410 | Common:4; Rare:125; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68030390-68030736 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68036316-68036552 | Rare:85; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:68271930-68272102 | Common:2; Rare:78 | ||||
| chr11:68903779-68903946 | Common:4; Rare:81; Clinvar (benign):6 | ||||
| chr11:69048728-69048960 | Common:5; Rare:82 | ||||
| chr11:69675251-69675502 | Rare:78 |