| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66843349-66843467 | Common:5; Rare:60 | ||||
| chr11:67317691-67317915 | Rare:52 | ||||
| chr11:67353277-67353386 | Rare:34 | ||||
| chr11:67353473-67353847 | Common:2; Rare:93 | ||||
| chr11:67401780-67402075 | Common:3; Rare:111 | ||||
| chr11:67428336-67428537 | Rare:69 | ||||
| chr11:67443423-67443697 | Common:2; Rare:94 | ||||
| chr11:67469222-67469407 | Common:1; Rare:54 | ||||
| chr11:67482910-67483170 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67629375-67629467 | Common:1; Rare:16 | ||||
| chr11:68010153-68010354 | Common:1; Rare:50 | ||||
| chr11:68030370-68030744 | Common:3; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039073 | Rare:46; Clinvar:1 | ||||
| chr11:68271871-68272192 | Common:2; Rare:134 | ||||
| chr11:68460223-68460309 | Common:2; Rare:46 |