| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126268814-126269192 | Common:1; Rare:145; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126283013-126283122 | Common:1; Rare:43 | ||||
| chr11:126304013-126304083 | Rare:38 | ||||
| chr11:126355482-126355778 | Common:2; Rare:83 | ||||
| chr11:128522272-128522596 | Common:3; Rare:105 | ||||
| chr11:129815689-129815877 | Common:1; Rare:47 | ||||
| chr11:129895535-129895687 | Common:2; Rare:57 | ||||
| chr11:130069551-130070002 | Common:2; Rare:169 | ||||
| chr11:130314395-130314521 | Common:1; Rare:42 | ||||
| chr11:130916394-130916627 | Common:7; Rare:76 | ||||
| chr11:134148290-134148574 | Rare:91 | ||||
| chr11:134223922-134224163 | Common:2; Rare:79 | ||||
| chr11:134224533-134224680 | Rare:52 | ||||
| chr11:134253254-134253586 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr12:389236-389364 | Rare:46 |