| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44066006-44066346 | Common:6; Rare:147 | ||||
| chr11:45147100-45147440 | Common:2; Rare:262 | ||||
| chr11:45804276-45804407 | Common:1; Rare:31 | ||||
| chr11:45804890-45805510 | Common:7; Rare:221; Clinvar:14; Clinvar (benign):3 | ||||
| chr11:45847227-45847492 | Common:4; Rare:206 | ||||
| chr11:45917804-45917923 | Rare:35 | ||||
| chr11:45918005-45918181 | Common:2; Rare:70; Clinvar (benign):2 | ||||
| chr11:46119122-46119670 | Common:3; Rare:159 | ||||
| chr11:46120952-46121350 | Common:4; Rare:94 | ||||
| chr11:46121386-46121707 | Rare:165 | ||||
| chr11:46344980-46345443 | Common:3; Rare:184 | ||||
| chr11:46347216-46347574 | Common:4; Rare:220 | ||||
| chr11:46381535-46381779 | Common:2; Rare:121 | ||||
| chr11:46593559-46593959 | Rare:126 | ||||
| chr11:46593881-46594223 | Common:4; Rare:135 |