| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700555-46700796 | Common:1; Rare:65 | ||||
| chr11:46846198-46846414 | Common:1; Rare:63 | ||||
| chr11:47185316-47185660 | Common:2; Rare:67 | ||||
| chr11:47248785-47248957 | Rare:71 | ||||
| chr11:47269974-47270212 | Common:1; Rare:84 | ||||
| chr11:47426307-47426648 | Common:1; Rare:88 | ||||
| chr11:47565478-47565621 | Common:3; Rare:29 | ||||
| chr11:47578940-47579100 | Rare:85; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47767305-47767456 | Rare:65 | ||||
| chr11:57324862-57325183 | Common:2; Rare:104 | ||||
| chr11:57427064-57427214 | Common:1; Rare:50 | ||||
| chr11:57514839-57514962 | Rare:19 | ||||
| chr11:57530682-57531052 | Common:1; Rare:92 | ||||
| chr11:57668039-57668153 | Rare:48 | ||||
| chr11:57712175-57712671 | Common:9; Rare:171 |