| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47408114-47408520 | Common:2; Rare:111 | ||||
| chr11:47426369-47426648 | Common:1; Rare:71 | ||||
| chr11:47552828-47552970 | Common:1; Rare:48 | ||||
| chr11:47553112-47553393 | Common:1; Rare:86 | ||||
| chr11:47565450-47565658 | Common:3; Rare:40 | ||||
| chr11:47578642-47578765 | Rare:28 | ||||
| chr11:47578917-47579100 | Rare:95; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642448-47642963 | Rare:159 | ||||
| chr11:47767211-47767735 | Common:2; Rare:173 | ||||
| chr11:47848275-47848452 | Common:1; Rare:95 | ||||
| chr11:47848490-47848750 | Common:3; Rare:56 | ||||
| chr11:47980305-47980577 | Common:2; Rare:88 | ||||
| chr11:57322657-57322805 | Rare:37 | ||||
| chr11:57324937-57325342 | Common:3; Rare:119 | ||||
| chr11:57335858-57335980 | Common:1; Rare:20 |