| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33736391-33736605 | Common:2; Rare:66 | ||||
| chr11:34052117-34052483 | Common:4; Rare:168 | ||||
| chr11:34105520-34105719 | Common:2; Rare:67 | ||||
| chr11:34916311-34916658 | Common:10; Rare:141; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35525590-35525816 | Rare:53 | ||||
| chr11:35943911-35944119 | Common:3; Rare:68 | ||||
| chr11:36510236-36510377 | Rare:40 | ||||
| chr11:43358839-43359001 | Rare:80 | ||||
| chr11:43880752-43880884 | Common:2; Rare:28 | ||||
| chr11:46617201-46617599 | Common:5; Rare:111 | ||||
| chr11:46700559-46700853 | Common:1; Rare:78 | ||||
| chr11:46700895-46701077 | Common:3; Rare:44 | ||||
| chr11:46846224-46846421 | Common:1; Rare:56 | ||||
| chr11:47269981-47270172 | Common:1; Rare:65 | ||||
| chr11:47426406-47426648 | Rare:60 |