| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214834-47215106 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:47248791-47248941 | Rare:60 | ||||
| chr11:47269523-47269700 | Common:1; Rare:56 | ||||
| chr11:47270012-47270184 | Common:1; Rare:59 | ||||
| chr11:47553008-47553356 | Common:3; Rare:121 | ||||
| chr11:47565521-47565643 | Common:2; Rare:22 | ||||
| chr11:47578943-47579094 | Rare:78; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47715350-47715411 | Common:1; Rare:18 | ||||
| chr11:47848314-47848394 | Rare:43 | ||||
| chr11:57324890-57325164 | Common:1; Rare:85 | ||||
| chr11:57335067-57335363 | Rare:60 | ||||
| chr11:57427085-57427187 | Common:1; Rare:31 | ||||
| chr11:57567605-57567767 | Rare:52 | ||||
| chr11:57567920-57567957 | Rare:8 | ||||
| chr11:57597573-57597711 | Rare:32; Clinvar:3; Clinvar (benign):1 |