| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31811237-31811479 | Rare:39; Clinvar:1 | ||||
| chr11:32583677-32583929 | Rare:92 | ||||
| chr11:33039474-33039799 | Common:1; Rare:79 | ||||
| chr11:33161435-33161678 | Common:6; Rare:68 | ||||
| chr11:33257157-33257434 | Common:3; Rare:97 | ||||
| chr11:33736391-33736569 | Common:2; Rare:59 | ||||
| chr11:33774454-33774666 | Common:2; Rare:78 | ||||
| chr11:34051622-34051741 | Rare:53 | ||||
| chr11:34105471-34105724 | Common:2; Rare:86 | ||||
| chr11:34438784-34439009 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr11:34916287-34916719 | Common:11; Rare:176; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35139075-35139181 | Rare:19 | ||||
| chr11:35418996-35419043 | Rare:12 | ||||
| chr11:35419525-35419685 | Rare:32 | ||||
| chr11:35525729-35525821 | Rare:13 |