| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:12207479-12207706 | Common:1; Rare:45 | ||||
| chr11:12377472-12377777 | Rare:107 | ||||
| chr11:13463147-13463374 | Common:1; Rare:83 | ||||
| chr11:14520300-14520594 | Rare:96 | ||||
| chr11:14643631-14643774 | Common:1; Rare:64 | ||||
| chr11:14892209-14892549 | Rare:90 | ||||
| chr11:16606061-16606159 | Common:1; Rare:19 | ||||
| chr11:16607817-16607893 | Rare:12 | ||||
| chr11:16612950-16613167 | Common:1; Rare:37 | ||||
| chr11:16738466-16738729 | Common:3; Rare:57 | ||||
| chr11:17077617-17077847 | Common:2; Rare:95 | ||||
| chr11:17207920-17208111 | Common:1; Rare:72 | ||||
| chr11:17276479-17276823 | Common:5; Rare:101; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 | ||||
| chr11:18322128-18322289 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):2 |