| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:27506737-27506838 | Common:1; Rare:46 | ||||
| chr11:31509576-31509784 | Common:1; Rare:65 | ||||
| chr11:33161478-33161678 | Common:5; Rare:55 | ||||
| chr11:33736391-33736514 | Common:2; Rare:40 | ||||
| chr11:34916351-34916650 | Common:8; Rare:117; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr11:46846254-46846414 | Common:1; Rare:44 | ||||
| chr11:47565522-47565620 | Common:2; Rare:18 | ||||
| chr11:47578968-47579085 | Rare:60; Clinvar:2 | ||||
| chr11:57712279-57712607 | Common:3; Rare:86 | ||||
| chr11:59142700-59142872 | Rare:22 | ||||
| chr11:61333065-61333240 | Rare:55 | ||||
| chr11:61361875-61361973 | Common:1; Rare:23 | ||||
| chr11:61362288-61362393 | Common:1; Rare:30; Clinvar:4 | ||||
| chr11:61429985-61430140 | Common:1; Rare:66; Clinvar (benign):2 | ||||
| chr11:61792573-61792908 | Common:5; Rare:86 |