| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47565499-47565796 | Common:4; Rare:71 | ||||
| chr11:47578637-47578871 | Rare:48 | ||||
| chr11:47578920-47579097 | Rare:91; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642462-47642799 | Rare:123 | ||||
| chr11:47848322-47848404 | Rare:40 | ||||
| chr11:47848504-47848617 | Common:2; Rare:21 | ||||
| chr11:57335731-57335996 | Common:4; Rare:54 | ||||
| chr11:57427085-57427214 | Common:1; Rare:37 | ||||
| chr11:57530715-57531078 | Common:1; Rare:90 | ||||
| chr11:57567605-57567957 | Common:2; Rare:97 | ||||
| chr11:57657522-57657794 | Common:4; Rare:68 | ||||
| chr11:57712175-57712671 | Common:9; Rare:171 | ||||
| chr11:57741305-57741596 | Common:1; Rare:110 | ||||
| chr11:57761584-57761974 | Common:3; Rare:79 | ||||
| chr11:57763756-57763823 | Common:1; Rare:14 |