| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33774501-33774663 | Common:2; Rare:58 | ||||
| chr11:34052119-34052317 | Common:2; Rare:86 | ||||
| chr11:34105478-34105724 | Common:2; Rare:82 | ||||
| chr11:34438763-34438999 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr11:34916282-34916676 | Common:10; Rare:160; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:36289411-36289523 | Common:2; Rare:37 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358795-43358979 | Rare:89 | ||||
| chr11:43680523-43680804 | Rare:84 | ||||
| chr11:45917851-45918180 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:45918792-45918907 | Rare:37 | ||||
| chr11:46361441-46361619 | Rare:38 | ||||
| chr11:46617210-46617585 | Common:5; Rare:103 | ||||
| chr11:46700568-46700818 | Common:1; Rare:64 | ||||
| chr11:46846211-46846432 | Common:1; Rare:62 |