| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6319880-6320288 | Common:3; Rare:153 | ||||
| chr11:6320481-6320613 | Common:2; Rare:47 | ||||
| chr11:6320981-6321207 | Common:1; Rare:36 | ||||
| chr11:6390004-6390062 | Common:1; Rare:5 | ||||
| chr11:6390138-6390544 | Common:2; Rare:106 | ||||
| chr11:6402693-6402947 | Common:2; Rare:72 | ||||
| chr11:6473834-6474113 | Rare:86 | ||||
| chr11:6481245-6481665 | Common:5; Rare:160 | ||||
| chr11:6603485-6603880 | Common:4; Rare:115; Clinvar (benign):3 | ||||
| chr11:6604016-6604051 | Rare:4 | ||||
| chr11:6604364-6604546 | Rare:47 | ||||
| chr11:6611397-6611739 | Common:1; Rare:111 | ||||
| chr11:6612119-6612582 | Common:5; Rare:139 | ||||
| chr11:6612645-6612789 | Common:1; Rare:28; Clinvar:1 | ||||
| chr11:6619159-6619585 | Common:3; Rare:151; Clinvar:4; Clinvar (benign):14; Clinvar (pathogenic):2 |