| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:76770960-76771390 | Common:1; Rare:60 | ||||
| chr11:76772450-76772984 | Common:5; Rare:207 | ||||
| chr11:76773896-76774188 | Common:2; Rare:55 | ||||
| chr11:76785364-76786026 | Common:8; Rare:184 | ||||
| chr11:76788428-76788615 | Common:1; Rare:27 | ||||
| chr11:76788660-76789150 | Common:3; Rare:153 | ||||
| chr11:77088450-77088970 | Common:6; Rare:86 | ||||
| chr11:77191589-77191775 | Common:2; Rare:42 | ||||
| chr11:77192061-77192293 | Common:1; Rare:85; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
| chr11:77590160-77590470 | Common:2; Rare:91 | ||||
| chr11:77819338-77819812 | Rare:163 | ||||
| chr11:77885967-77886684 | Common:9; Rare:263 | ||||
| chr11:78030450-78030950 | Common:2; Rare:92 | ||||
| chr11:78040084-78040235 | Rare:26 | ||||
| chr11:78155880-78156540 | Common:1; Rare:98 |