| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68903770-68903943 | Common:4; Rare:81; Clinvar (benign):6 | ||||
| chr11:70270440-70270801 | Common:2; Rare:142 | ||||
| chr11:70398421-70398623 | Common:2; Rare:74 | ||||
| chr11:70416822-70417123 | Common:3; Rare:97 | ||||
| chr11:71448347-71448679 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787350-71787537 | Common:11; Rare:75 | ||||
| chr11:71928682-71929064 | Common:1; Rare:107 | ||||
| chr11:72009122-72009234 | Rare:45 | ||||
| chr11:72040972-72041175 | Common:1; Rare:39 | ||||
| chr11:72080232-72080341 | Common:6; Rare:15 | ||||
| chr11:72080420-72080819 | Common:2; Rare:96; Clinvar:7 | ||||
| chr11:72103193-72103628 | Rare:113 | ||||
| chr11:72112241-72112530 | Rare:72 | ||||
| chr11:72223791-72223946 | Rare:43 | ||||
| chr11:72228989-72229227 | Rare:67; Clinvar (pathogenic):1 |