| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:637821-638001 | Common:4; Rare:51 | ||||
| chr11:638396-638508 | Rare:32 | ||||
| chr11:639834-639893 | Rare:26 | ||||
| chr11:639897-640232 | Common:15; Rare:222 | ||||
| chr11:748069-748215 | Rare:26 | ||||
| chr11:819722-819856 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:820034-820275 | Common:2; Rare:49 | ||||
| chr11:897297-897416 | Rare:26 | ||||
| chr11:1044189-1044228 | Rare:4 | ||||
| chr11:1262624-1262866 | Common:3; Rare:67 | ||||
| chr11:1271037-1271060 | Rare:5 | ||||
| chr11:1335627-1336027 | Common:2; Rare:69 | ||||
| chr11:1336508-1336697 | Common:1; Rare:17 | ||||
| chr11:1382940-1383301 | Common:2; Rare:101 | ||||
| chr11:1383303-1383484 | Common:1; Rare:41 |