| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:4393646-4393820 | Rare:43 | ||||
| chr11:5596597-5596773 | Common:4; Rare:63 | ||||
| chr11:5624889-5625044 | Rare:27 | ||||
| chr11:6234592-6234876 | Common:2; Rare:90 | ||||
| chr11:6320490-6320558 | Common:2; Rare:23 | ||||
| chr11:6390237-6390600 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:6390679-6390910 | Common:6; Rare:108; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr11:6473834-6474124 | Rare:89 | ||||
| chr11:6481274-6481569 | Common:5; Rare:132 | ||||
| chr11:6603521-6603835 | Common:4; Rare:94; Clinvar (benign):3 | ||||
| chr11:6619197-6619476 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:6682763-6683081 | Common:2; Rare:85 | ||||
| chr11:6683197-6683650 | Common:6; Rare:172 | ||||
| chr11:7020316-7020462 | Rare:48 | ||||
| chr11:7513617-7514078 | Common:6; Rare:138 |