| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125625871-125625993 | Rare:40 | ||||
| chr11:125887436-125887737 | Common:2; Rare:93 | ||||
| chr11:126211624-126211804 | Rare:83 | ||||
| chr11:126268779-126269192 | Common:1; Rare:158; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126304033-126304083 | Rare:30 | ||||
| chr11:126355526-126355763 | Common:2; Rare:66 | ||||
| chr11:129024108-129024246 | Common:1; Rare:24 | ||||
| chr11:129815769-129815906 | Common:1; Rare:36 | ||||
| chr11:129895535-129895677 | Common:2; Rare:54 | ||||
| chr11:130002799-130002903 | Common:1; Rare:18 | ||||
| chr11:130069628-130069932 | Common:2; Rare:109 | ||||
| chr11:130314414-130314495 | Common:1; Rare:22 | ||||
| chr11:134225448-134225550 | Rare:29 | ||||
| chr11:134253278-134253592 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr12:389242-389383 | Rare:53 |