| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:27506748-27506875 | Common:1; Rare:53 | ||||
| chr11:28108115-28108414 | Common:1; Rare:90 | ||||
| chr11:30323030-30323164 | Common:1; Rare:42 | ||||
| chr11:31369731-31369882 | Rare:45 | ||||
| chr11:31509575-31509796 | Common:1; Rare:71 | ||||
| chr11:33161440-33161682 | Common:6; Rare:68 | ||||
| chr11:33257157-33257427 | Common:3; Rare:92 | ||||
| chr11:33258136-33258346 | Rare:82 | ||||
| chr11:34438784-34439007 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr11:34916311-34916658 | Common:10; Rare:141; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138954-35139260 | Common:1; Rare:74 | ||||
| chr11:35943932-35944125 | Common:3; Rare:64 | ||||
| chr11:36510235-36510372 | Rare:38 | ||||
| chr11:43311758-43312064 | Common:2; Rare:99 | ||||
| chr11:45917866-45918163 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 |