| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47426420-47426661 | Rare:58 | ||||
| chr11:47552666-47552790 | Common:1; Rare:52 | ||||
| chr11:47553065-47553393 | Common:2; Rare:111 | ||||
| chr11:47565320-47565795 | Common:4; Rare:100 | ||||
| chr11:47566131-47566263 | Rare:23 | ||||
| chr11:47578958-47579161 | Rare:101; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642079-47642257 | Rare:46 | ||||
| chr11:47642266-47642336 | Rare:19 | ||||
| chr11:47642356-47642898 | Rare:163 | ||||
| chr11:47715279-47715469 | Common:1; Rare:53 | ||||
| chr11:47767193-47767767 | Common:2; Rare:197 | ||||
| chr11:47848223-47848438 | Common:1; Rare:108 | ||||
| chr11:47848527-47848711 | Common:3; Rare:44 | ||||
| chr11:57311451-57311726 | Common:1; Rare:70 | ||||
| chr11:57325135-57325357 | Common:2; Rare:62 |