| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:809492-809665 | Common:2; Rare:51 | ||||
| chr11:809799-810038 | Common:2; Rare:110 | ||||
| chr11:818701-818946 | Rare:53; Clinvar:1 | ||||
| chr11:832866-833022 | Common:7; Rare:57 | ||||
| chr11:842413-842984 | Common:8; Rare:231 | ||||
| chr11:843963-844183 | Common:1; Rare:53 | ||||
| chr11:844186-844442 | Common:3; Rare:78 | ||||
| chr11:1036718-1036747 | Rare:6 | ||||
| chr11:1309535-1309851 | Common:3; Rare:132 | ||||
| chr11:1838615-1839033 | Common:2; Rare:111; Clinvar:1 | ||||
| chr11:1853035-1853175 | Common:2; Rare:47 | ||||
| chr11:1871152-1871376 | Common:3; Rare:65 | ||||
| chr11:1876442-1876495 | Rare:10 | ||||
| chr11:1919357-1919761 | Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:1922613-1922886 | Common:1; Rare:78 |