Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:46119792-46120141 | Common:3; Rare:77 | ||||
chr11:46381975-46382129 | Common:1; Rare:62 | ||||
chr11:46617210-46617585 | Common:5; Rare:103 | ||||
chr11:46700555-46700815 | Common:1; Rare:68 | ||||
chr11:46700925-46701068 | Common:2; Rare:41 | ||||
chr11:46846211-46846412 | Common:1; Rare:55 | ||||
chr11:47214843-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
chr11:47248762-47248938 | Rare:69 | ||||
chr11:47269978-47270184 | Common:1; Rare:69 | ||||
chr11:47426406-47426639 | Rare:59 | ||||
chr11:47553078-47553309 | Common:2; Rare:85 | ||||
chr11:47565471-47565640 | Common:3; Rare:32 | ||||
chr11:47578959-47579113 | Rare:80; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr11:47642473-47642721 | Rare:102 | ||||
chr11:47848317-47848385 | Rare:37 |