| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65663087-65663480 | Common:7; Rare:160 | ||||
| chr11:65711849-65712428 | Common:2; Rare:390 | ||||
| chr11:65720408-65720588 | Common:2; Rare:169; Clinvar:1 | ||||
| chr11:65780791-65780977 | Common:1; Rare:59 | ||||
| chr11:65856960-65857370 | Common:5; Rare:209 | ||||
| chr11:65859312-65859712 | Rare:166 | ||||
| chr11:65860224-65860872 | Common:7; Rare:347 | ||||
| chr11:65861070-65861530 | Common:5; Rare:190 | ||||
| chr11:65873520-65873840 | Common:6; Rare:180 | ||||
| chr11:65888392-65888690 | Common:2; Rare:203 | ||||
| chr11:65890452-65890703 | Common:7; Rare:147 | ||||
| chr11:65900317-65900450 | Common:4; Rare:25 | ||||
| chr11:65919003-65919533 | Common:1; Rare:372 | ||||
| chr11:65961496-65961782 | Common:1; Rare:145 | ||||
| chr11:66002074-66002395 | Common:4; Rare:152; Clinvar:12; Clinvar (benign):4 |