| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67650656-67650792 | Common:2; Rare:27 | ||||
| chr11:68030381-68030736 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038924-68039060 | Rare:40; Clinvar:1 | ||||
| chr11:68271900-68272134 | Common:2; Rare:97 | ||||
| chr11:68903779-68903943 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69640990-69641261 | Common:1; Rare:57 | ||||
| chr11:69675306-69675519 | Rare:56 | ||||
| chr11:70398349-70398596 | Common:2; Rare:86 | ||||
| chr11:71448338-71448690 | Common:4; Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787317-71787537 | Common:12; Rare:84 | ||||
| chr11:71928930-71929071 | Common:1; Rare:47 | ||||
| chr11:72040998-72041243 | Common:1; Rare:46 | ||||
| chr11:72041534-72041602 | Rare:6 | ||||
| chr11:72041846-72041889 | Common:1; Rare:9 | ||||
| chr11:72041933-72042018 | Rare:15 |