| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47578959-47579106 | Rare:74; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642453-47642696 | Rare:100 | ||||
| chr11:47767201-47767470 | Common:1; Rare:119 | ||||
| chr11:57324860-57325183 | Common:2; Rare:104 | ||||
| chr11:57514858-57514968 | Rare:20 | ||||
| chr11:57530703-57530850 | Common:1; Rare:37 | ||||
| chr11:57567589-57567758 | Rare:59 | ||||
| chr11:57597568-57597725 | Rare:39; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:57606007-57606547 | Rare:145; Clinvar (benign):2 | ||||
| chr11:57712023-57712657 | Common:10; Rare:214 | ||||
| chr11:58578085-58578138 | Rare:15 | ||||
| chr11:58578147-58578498 | Common:4; Rare:111 | ||||
| chr11:58578811-58579224 | Common:6; Rare:120 | ||||
| chr11:59142694-59142951 | Common:1; Rare:46 | ||||
| chr11:59212872-59213060 | Rare:50 |