Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:121210059-121210146 | Common:2; Rare:30 | ||||
chr12:121399809-121400154 | Common:5; Rare:127 | ||||
chr12:121672624-121672702 | Common:4; Rare:27 | ||||
chr12:121802940-121803109 | Common:1; Rare:40 | ||||
chr12:122266417-122266553 | Common:2; Rare:55 | ||||
chr12:122526885-122527282 | Common:3; Rare:138 | ||||
chr12:122896064-122896212 | Rare:80 | ||||
chr12:122980584-122980833 | Common:1; Rare:84 | ||||
chr12:123233093-123233512 | Common:2; Rare:143; Clinvar:1 | ||||
chr12:123364828-123364977 | Common:3; Rare:57 | ||||
chr12:123584334-123584609 | Common:5; Rare:91 | ||||
chr12:123601854-123602139 | Common:6; Rare:73 | ||||
chr12:123633632-123633856 | Common:1; Rare:103; Clinvar:8; Clinvar (benign):1 | ||||
chr12:123972565-123972899 | Common:6; Rare:114 | ||||
chr12:124388815-124388988 | Common:3; Rare:52 |