| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6319793-6320286 | Common:3; Rare:167 | ||||
| chr11:6320481-6320627 | Common:2; Rare:51 | ||||
| chr11:6390189-6390431 | Common:2; Rare:68 | ||||
| chr11:6419056-6419423 | Common:4; Rare:96 | ||||
| chr11:6473835-6474162 | Common:1; Rare:99 | ||||
| chr11:6481285-6481663 | Common:5; Rare:149 | ||||
| chr11:6603546-6603817 | Common:4; Rare:82; Clinvar (benign):3 | ||||
| chr11:6604080-6604750 | Common:3; Rare:218; Clinvar (benign):6 | ||||
| chr11:6612169-6612500 | Common:4; Rare:96 | ||||
| chr11:6619358-6619570 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6683286-6683691 | Common:6; Rare:145 | ||||
| chr11:6926339-6926583 | Common:5; Rare:70 | ||||
| chr11:6926701-6927101 | Common:6; Rare:147 | ||||
| chr11:7020308-7020483 | Rare:59 | ||||
| chr11:7513638-7514059 | Common:5; Rare:123 |