| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69675300-69675503 | Rare:57 | ||||
| chr11:70398421-70398596 | Common:2; Rare:63 | ||||
| chr11:70826507-70826587 | Rare:26 | ||||
| chr11:71448352-71448686 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71452987-71453249 | Common:3; Rare:72 | ||||
| chr11:71787349-71787564 | Common:13; Rare:95 | ||||
| chr11:71928930-71929079 | Common:1; Rare:49 | ||||
| chr11:72040686-72040916 | Rare:45 | ||||
| chr11:72041015-72041241 | Common:1; Rare:40 | ||||
| chr11:72041512-72041587 | Rare:10 | ||||
| chr11:72041846-72041893 | Common:1; Rare:9 | ||||
| chr11:72041902-72042016 | Rare:24 | ||||
| chr11:72080427-72080867 | Common:2; Rare:105; Clinvar:9 | ||||
| chr11:72223786-72223927 | Rare:41 | ||||
| chr11:72752382-72752572 | Common:3; Rare:56 |