| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70085299-70085490 | Common:1; Rare:35 | ||||
| chr11:70165070-70165191 | Common:2; Rare:33 | ||||
| chr11:70203133-70203343 | Common:3; Rare:79 | ||||
| chr11:70327349-70327568 | Common:3; Rare:39 | ||||
| chr11:70340897-70341013 | Common:2; Rare:21 | ||||
| chr11:70398349-70398614 | Common:2; Rare:96 | ||||
| chr11:71448328-71448708 | Common:4; Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452963-71453284 | Common:4; Rare:88 | ||||
| chr11:71787374-71787564 | Common:12; Rare:95 | ||||
| chr11:71928390-71929118 | Common:1; Rare:205 | ||||
| chr11:72039802-72039932 | Common:1; Rare:20 | ||||
| chr11:72040964-72041167 | Common:1; Rare:39 | ||||
| chr11:72041512-72041549 | Rare:8 | ||||
| chr11:72041846-72041936 | Common:2; Rare:20 | ||||
| chr11:72041949-72042061 | Rare:26 |