| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44726370-44726516 | Common:1; Rare:35 | ||||
| chr11:45146561-45146728 | Common:2; Rare:40 | ||||
| chr11:45146898-45146921 | Rare:3 | ||||
| chr11:45147082-45147374 | Common:1; Rare:123 | ||||
| chr11:45804258-45804476 | Common:1; Rare:46 | ||||
| chr11:45804882-45805286 | Common:3; Rare:103; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:45847123-45847546 | Common:2; Rare:165 | ||||
| chr11:45917210-45917486 | Common:1; Rare:68; Clinvar:2 | ||||
| chr11:45917756-45918201 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45918774-45918905 | Rare:40 | ||||
| chr11:46119568-46119635 | Common:1; Rare:18 | ||||
| chr11:46121318-46121625 | Rare:77 | ||||
| chr11:46345197-46345482 | Common:1; Rare:81 | ||||
| chr11:46347213-46347570 | Common:2; Rare:112 | ||||
| chr11:46361401-46361634 | Rare:51 |