Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:126211610-126211804 | Rare:90 | ||||
chr11:126268814-126269207 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):4 | ||||
chr11:126303825-126304073 | Rare:91 | ||||
chr11:126355532-126355742 | Common:1; Rare:54 | ||||
chr11:128522267-128522566 | Common:1; Rare:94 | ||||
chr11:128693210-128693269 | Common:1; Rare:19 | ||||
chr11:128693944-128694241 | Rare:55 | ||||
chr11:130002780-130002966 | Common:3; Rare:33 | ||||
chr11:130069654-130069928 | Common:1; Rare:96 | ||||
chr11:130071047-130071253 | Common:1; Rare:42 | ||||
chr11:130314386-130314495 | Common:1; Rare:32 | ||||
chr11:130314724-130315040 | Common:4; Rare:109 | ||||
chr11:134224530-134224695 | Rare:62 | ||||
chr11:134253297-134253603 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
chr12:168908-169011 | Common:2; Rare:27 |