Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189784268-189784512 | Common:3; Rare:83; Clinvar:7; Clinvar (benign):2 | ||||
chr2:190343864-190343938 | Rare:13 | ||||
chr2:191677856-191678147 | Common:4; Rare:82 | ||||
chr2:197434973-197435182 | Rare:71 | ||||
chr2:197499813-197500214 | Rare:147; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197500258-197500418 | Common:1; Rare:65 | ||||
chr2:200306217-200306574 | Common:5; Rare:88 | ||||
chr2:200864211-200864264 | Rare:19 | ||||
chr2:200889011-200889439 | Common:3; Rare:140 | ||||
chr2:200963622-200963884 | Common:1; Rare:65 | ||||
chr2:201071598-201072052 | Rare:99 | ||||
chr2:201118628-201118825 | Rare:30 | ||||
chr2:201122433-201122621 | Common:1; Rare:39 | ||||
chr2:201451542-201451820 | Common:2; Rare:74 | ||||
chr2:201642660-201642743 | Rare:43 |