| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34916280-34916669 | Common:10; Rare:158; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:36510230-36510377 | Rare:44 | ||||
| chr11:43358795-43358970 | Rare:81 | ||||
| chr11:43880752-43880877 | Common:2; Rare:25 | ||||
| chr11:45917865-45918146 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46617210-46617580 | Common:5; Rare:103 | ||||
| chr11:46846218-46846394 | Rare:46 | ||||
| chr11:47186408-47186542 | Rare:37 | ||||
| chr11:47214833-47215115 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248793-47248913 | Rare:46 | ||||
| chr11:47269971-47270166 | Common:1; Rare:64 | ||||
| chr11:47553071-47553347 | Common:2; Rare:101 | ||||
| chr11:47565483-47565643 | Common:3; Rare:31 | ||||
| chr11:47578952-47579089 | Rare:70; Clinvar:2 | ||||
| chr11:47642461-47642793 | Rare:123 |