| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401789-67402075 | Common:3; Rare:103 | ||||
| chr11:67428220-67428537 | Rare:103 | ||||
| chr11:67469225-67469407 | Common:1; Rare:52 | ||||
| chr11:67482926-67483157 | Rare:54; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508627-67508778 | Common:3; Rare:54 | ||||
| chr11:68010117-68010354 | Common:1; Rare:62 | ||||
| chr11:68030390-68030744 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039073 | Rare:47; Clinvar:1 | ||||
| chr11:68213575-68213729 | Rare:89 | ||||
| chr11:68271895-68272134 | Common:2; Rare:100 | ||||
| chr11:68903791-68903943 | Common:4; Rare:69; Clinvar (benign):6 | ||||
| chr11:69640952-69641218 | Rare:58 | ||||
| chr11:69675324-69675534 | Common:1; Rare:54 | ||||
| chr11:70398455-70398596 | Common:1; Rare:46 | ||||
| chr11:71448311-71448720 | Common:5; Rare:109; Clinvar:3; Clinvar (benign):1 |