| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401783-67402071 | Common:3; Rare:108 | ||||
| chr11:67428295-67428531 | Rare:82 | ||||
| chr11:67482915-67483164 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68030393-68030744 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271910-68272065 | Common:1; Rare:72 | ||||
| chr11:68460560-68460773 | Common:3; Rare:79 | ||||
| chr11:68903791-68903938 | Common:4; Rare:67; Clinvar (benign):6 | ||||
| chr11:69675324-69675478 | Rare:41 | ||||
| chr11:70398431-70398596 | Common:2; Rare:58 | ||||
| chr11:71448352-71448640 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71452987-71453258 | Common:3; Rare:76 | ||||
| chr11:71928889-71929058 | Common:1; Rare:58 | ||||
| chr11:72041056-72041280 | Common:1; Rare:38 | ||||
| chr11:72041846-72041889 | Common:1; Rare:9 | ||||
| chr11:72080502-72080867 | Common:1; Rare:81; Clinvar:6 |