| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67303343-67303567 | Rare:59 | ||||
| chr11:67317283-67317683 | Common:1; Rare:151 | ||||
| chr11:67317730-67317915 | Rare:75 | ||||
| chr11:67353483-67353867 | Common:4; Rare:183 | ||||
| chr11:67374080-67374570 | Rare:116 | ||||
| chr11:67401773-67402108 | Common:6; Rare:230 | ||||
| chr11:67403550-67403990 | Rare:138 | ||||
| chr11:67421100-67421500 | Common:9; Rare:234 | ||||
| chr11:67428241-67428546 | Rare:160 | ||||
| chr11:67443436-67443628 | Common:2; Rare:131 | ||||
| chr11:67443790-67443970 | Rare:51 | ||||
| chr11:67464630-67464855 | Rare:252 | ||||
| chr11:67469212-67469417 | Common:2; Rare:123 | ||||
| chr11:67482947-67483164 | Rare:93; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:67505312-67505456 | Rare:37 |