Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:11171547-11171723 | Common:2; Rare:57 | ||||
chr12:11649752-11650158 | Common:1; Rare:119 | ||||
chr12:12356970-12357212 | Common:4; Rare:121 | ||||
chr12:12560864-12561183 | Common:4; Rare:70 | ||||
chr12:12562224-12562333 | Rare:32 | ||||
chr12:12611809-12612153 | Common:2; Rare:101 | ||||
chr12:12717821-12717873 | Rare:23; Clinvar:6; Clinvar (benign):3 | ||||
chr12:12725649-12725959 | Common:3; Rare:70 | ||||
chr12:12891272-12891695 | Common:2; Rare:84 | ||||
chr12:13000174-13000476 | Common:2; Rare:94 | ||||
chr12:14567604-14567820 | Common:7; Rare:65 | ||||
chr12:14774184-14774732 | Common:3; Rare:167 | ||||
chr12:14803403-14803687 | Common:2; Rare:76 | ||||
chr12:14961546-14961765 | Common:2; Rare:54 | ||||
chr12:15882308-15882655 | Common:1; Rare:99 |