Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:34105442-34105792 | Common:4; Rare:113 | ||||
chr11:34438802-34439009 | Common:2; Rare:70; Clinvar (benign):1 | ||||
chr11:34439138-34439443 | Common:4; Rare:67 | ||||
chr11:34916282-34916618 | Common:8; Rare:137; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr11:34977532-34977864 | Rare:68 | ||||
chr11:35138637-35138916 | Common:2; Rare:61 | ||||
chr11:35138949-35139264 | Common:1; Rare:76 | ||||
chr11:35139267-35139366 | Rare:39 | ||||
chr11:35205149-35205419 | Common:2; Rare:45 | ||||
chr11:35205507-35205815 | Rare:51 | ||||
chr11:35525532-35525652 | Rare:39 | ||||
chr11:35663237-35663756 | Rare:179; Clinvar (pathogenic):1 | ||||
chr11:35943949-35944056 | Common:2; Rare:38 | ||||
chr11:36510236-36510372 | Rare:38 | ||||
chr11:43358827-43359106 | Rare:114 |