| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3856063-3856308 | Rare:77; Clinvar:1 | ||||
| chr11:4094543-4094982 | Common:2; Rare:118 | ||||
| chr11:4393654-4393803 | Rare:35 | ||||
| chr11:5596617-5596727 | Common:3; Rare:41 | ||||
| chr11:5624893-5625033 | Rare:22 | ||||
| chr11:6390219-6390502 | Common:2; Rare:82 | ||||
| chr11:6473884-6474085 | Rare:65 | ||||
| chr11:6481285-6481545 | Common:4; Rare:114 | ||||
| chr11:6603536-6603860 | Common:4; Rare:97; Clinvar (benign):3 | ||||
| chr11:6614929-6615157 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:6619200-6619560 | Common:3; Rare:127; Clinvar:4; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:6683249-6683637 | Common:6; Rare:151 | ||||
| chr11:6926120-6926463 | Common:4; Rare:87 | ||||
| chr11:6926846-6926935 | Common:1; Rare:21 | ||||
| chr11:7513616-7514023 | Common:6; Rare:124 |