| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6473824-6473869 | Rare:9 | ||||
| chr11:6481276-6481585 | Common:5; Rare:133 | ||||
| chr11:6603521-6603860 | Common:4; Rare:100; Clinvar (benign):3 | ||||
| chr11:6603907-6604051 | Common:1; Rare:45 | ||||
| chr11:6604644-6605049 | Common:5; Rare:97 | ||||
| chr11:6612152-6612331 | Common:2; Rare:69 | ||||
| chr11:6615245-6615509 | Common:2; Rare:80; Clinvar:12; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr11:6619336-6619495 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6926254-6926472 | Common:4; Rare:62 | ||||
| chr11:6926853-6926879 | Rare:6 | ||||
| chr11:7513612-7514007 | Common:6; Rare:120 | ||||
| chr11:7597037-7597327 | Common:3; Rare:56 | ||||
| chr11:7673408-7673617 | Common:1; Rare:73 | ||||
| chr11:7677189-7677435 | Common:3; Rare:43 | ||||
| chr11:7965405-7965756 | Common:2; Rare:48 |