| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125111580-125111630 | Common:1; Rare:18 | ||||
| chr11:125592543-125592913 | Common:6; Rare:121 | ||||
| chr11:125625861-125625991 | Rare:42 | ||||
| chr11:125887495-125887727 | Common:2; Rare:72 | ||||
| chr11:126211644-126211810 | Rare:77 | ||||
| chr11:126268775-126269184 | Common:1; Rare:156; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126304017-126304105 | Rare:50 | ||||
| chr11:128522263-128522531 | Common:1; Rare:83 | ||||
| chr11:128692828-128692985 | Rare:41 | ||||
| chr11:128693817-128694120 | Common:2; Rare:56 | ||||
| chr11:130314416-130314519 | Common:1; Rare:33 | ||||
| chr11:130916421-130916629 | Common:5; Rare:68 | ||||
| chr11:131911364-131911492 | Common:1; Rare:56 | ||||
| chr11:134223930-134224166 | Common:2; Rare:76 | ||||
| chr11:134253254-134253586 | Common:2; Rare:106; Clinvar (benign):1 |