| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269513-47269714 | Common:1; Rare:68 | ||||
| chr11:47269986-47270212 | Common:1; Rare:82 | ||||
| chr11:47565460-47565625 | Common:3; Rare:32 | ||||
| chr11:47578947-47579319 | Rare:174; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:57324902-57325173 | Common:1; Rare:86 | ||||
| chr11:57712184-57712625 | Common:9; Rare:147 | ||||
| chr11:57741300-57741596 | Common:1; Rare:112 | ||||
| chr11:58578237-58578499 | Common:3; Rare:89 | ||||
| chr11:58578825-58579185 | Common:4; Rare:107 | ||||
| chr11:59142678-59142940 | Common:1; Rare:47 | ||||
| chr11:59668986-59669312 | Rare:113 | ||||
| chr11:60906426-60906656 | Rare:57 | ||||
| chr11:61161435-61161755 | Common:1; Rare:87 | ||||
| chr11:61333038-61333259 | Rare:74 | ||||
| chr11:61361870-61361950 | Rare:16 |