| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61754503-61754903 | Rare:167 | ||||
| chr11:61791813-61792546 | Common:1; Rare:220 | ||||
| chr11:61792523-61793144 | Common:37; Rare:833 | ||||
| chr11:61793235-61793848 | Common:1; Rare:143 | ||||
| chr11:61813947-61814917 | Common:8; Rare:327 | ||||
| chr11:61814973-61815694 | Common:23; Rare:551 | ||||
| chr11:61815771-61816469 | Rare:544 | ||||
| chr11:61816661-61817831 | Common:18; Rare:939 | ||||
| chr11:61890568-61891271 | Common:7; Rare:298 | ||||
| chr11:61891434-61891598 | Common:1; Rare:55 | ||||
| chr11:61891538-61892007 | Common:5; Rare:202 | ||||
| chr11:61916451-61918130 | Common:20; Rare:942 | ||||
| chr11:61920170-61920620 | Common:13; Rare:222 | ||||
| chr11:61949560-61950000 | Common:16; Rare:312; Clinvar (benign):1 | ||||
| chr11:61950063-61950463 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):3 |