| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34916295-34916664 | Common:10; Rare:151; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138971-35139201 | Common:1; Rare:51 | ||||
| chr11:35943975-35944087 | Common:1; Rare:36 | ||||
| chr11:36510229-36510377 | Rare:45 | ||||
| chr11:43358893-43358970 | Rare:43 | ||||
| chr11:43880709-43880877 | Common:2; Rare:37 | ||||
| chr11:46617222-46617585 | Common:5; Rare:99 | ||||
| chr11:46701020-46701045 | Rare:12 | ||||
| chr11:46846198-46846414 | Common:1; Rare:63 | ||||
| chr11:47214840-47215021 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:47269529-47269684 | Common:1; Rare:52 | ||||
| chr11:47553069-47553356 | Common:2; Rare:102 | ||||
| chr11:47565521-47565620 | Common:2; Rare:18 | ||||
| chr11:47578952-47579097 | Rare:74; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47848325-47848410 | Rare:44 |