| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125625871-125625968 | Rare:33 | ||||
| chr11:125887520-125887727 | Common:2; Rare:61 | ||||
| chr11:126211639-126211804 | Rare:75 | ||||
| chr11:126268805-126269199 | Common:1; Rare:154; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126303974-126304081 | Rare:61 | ||||
| chr11:126355545-126355768 | Rare:58 | ||||
| chr11:128693802-128694153 | Common:2; Rare:64 | ||||
| chr11:129895535-129895677 | Common:2; Rare:54 | ||||
| chr11:130314406-130314520 | Common:1; Rare:38 | ||||
| chr11:130448445-130448652 | Rare:50 | ||||
| chr11:131911263-131911460 | Common:1; Rare:66 | ||||
| chr11:134223922-134224103 | Common:2; Rare:54 | ||||
| chr11:134224537-134224615 | Rare:25 | ||||
| chr11:134253298-134253592 | Common:2; Rare:97; Clinvar (benign):1 | ||||
| chr12:389249-389347 | Rare:38 |