| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67303356-67303584 | Rare:60 | ||||
| chr11:67317734-67317915 | Rare:40 | ||||
| chr11:67356942-67357132 | Rare:34 | ||||
| chr11:67401528-67401939 | Common:2; Rare:148 | ||||
| chr11:67428340-67428572 | Rare:89 | ||||
| chr11:67443441-67443701 | Common:2; Rare:91 | ||||
| chr11:67464538-67464829 | Common:1; Rare:153 | ||||
| chr11:67469105-67469407 | Common:3; Rare:106 | ||||
| chr11:67482907-67483192 | Rare:63; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67506237-67506549 | Common:1; Rare:58 | ||||
| chr11:67507786-67507877 | Rare:22 | ||||
| chr11:67508030-67508468 | Common:1; Rare:100 | ||||
| chr11:67508618-67508795 | Common:3; Rare:65 | ||||
| chr11:67583551-67583909 | Common:2; Rare:106 | ||||
| chr11:67608223-67608438 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 |