| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47257450-47258010 | Common:2; Rare:178 | ||||
| chr11:47269024-47269396 | Common:1; Rare:105 | ||||
| chr11:47269440-47269820 | Common:2; Rare:181 | ||||
| chr11:47269974-47270184 | Common:2; Rare:137 | ||||
| chr11:47408348-47408653 | Common:3; Rare:188; Clinvar (benign):4 | ||||
| chr11:47426396-47426687 | Common:1; Rare:71 | ||||
| chr11:47565437-47565728 | Common:7; Rare:105 | ||||
| chr11:47578928-47579318 | Rare:255; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr11:47641900-47642130 | Rare:110 | ||||
| chr11:47642432-47642802 | Rare:236 | ||||
| chr11:47767178-47767705 | Common:4; Rare:329 | ||||
| chr11:47848305-47848623 | Common:2; Rare:173 | ||||
| chr11:47848531-47848661 | Common:3; Rare:26 | ||||
| chr11:47980297-47980748 | Common:4; Rare:219 | ||||
| chr11:57324861-57325267 | Common:3; Rare:215 |