| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125903112-125903328 | Rare:47 | ||||
| chr11:126062953-126062996 | Rare:16 | ||||
| chr11:126063009-126063065 | Rare:19 | ||||
| chr11:126211195-126211307 | Rare:22 | ||||
| chr11:126211310-126211464 | Common:1; Rare:47 | ||||
| chr11:126211564-126211882 | Rare:140 | ||||
| chr11:126211995-126212090 | Rare:24 | ||||
| chr11:126212146-126212211 | Rare:11 | ||||
| chr11:126268423-126268674 | Common:3; Rare:65 | ||||
| chr11:126268731-126269230 | Common:2; Rare:197; Clinvar:3; Clinvar (benign):6 | ||||
| chr11:126269369-126269387 | Rare:3 | ||||
| chr11:126282614-126282930 | Common:3; Rare:72 | ||||
| chr11:126282953-126283220 | Common:2; Rare:78 | ||||
| chr11:126283237-126283400 | Common:1; Rare:39 | ||||
| chr11:126283438-126283622 | Common:1; Rare:33 |