| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32434816-32435216 | Common:5; Rare:286; Clinvar:58; Clinvar (benign):30; Clinvar (pathogenic):1 | ||||
| chr11:32583700-32583932 | Rare:87 | ||||
| chr11:32829653-32829789 | Common:1; Rare:25 | ||||
| chr11:32892758-32893170 | Common:3; Rare:158 | ||||
| chr11:33015741-33015956 | Common:5; Rare:171 | ||||
| chr11:33038990-33039820 | Common:8; Rare:278 | ||||
| chr11:33039840-33040130 | Common:5; Rare:81 | ||||
| chr11:33161364-33161689 | Common:13; Rare:157 | ||||
| chr11:33257154-33257476 | Common:6; Rare:190 | ||||
| chr11:33258040-33258370 | Common:2; Rare:211 | ||||
| chr11:33699599-33699960 | Common:8; Rare:100 | ||||
| chr11:33700530-33701040 | Common:6; Rare:128 | ||||
| chr11:33736393-33736570 | Common:3; Rare:111 | ||||
| chr11:34051459-34051807 | Rare:206 | ||||
| chr11:34052062-34052467 | Common:9; Rare:330 |