| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62855881-62856161 | Rare:104 | ||||
| chr11:62880779-62880934 | Common:1; Rare:42 | ||||
| chr11:63974395-63974663 | Common:1; Rare:68 | ||||
| chr11:64226116-64226318 | Common:2; Rare:58 | ||||
| chr11:64240891-64241139 | Rare:67 | ||||
| chr11:64245842-64246004 | Common:1; Rare:37 | ||||
| chr11:64284643-64284854 | Common:1; Rare:96 | ||||
| chr11:64317475-64317681 | Common:4; Rare:68 | ||||
| chr11:64318035-64318328 | Common:1; Rare:134 | ||||
| chr11:65014069-65014230 | Rare:33 | ||||
| chr11:65084041-65084248 | Common:1; Rare:59 | ||||
| chr11:65134485-65134815 | Common:3; Rare:86 | ||||
| chr11:65314711-65314921 | Rare:75 | ||||
| chr11:65662902-65663062 | Common:1; Rare:43 | ||||
| chr11:66002120-66002552 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):3 |