Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206085765-206085981 | Common:1; Rare:62 | ||||
chr2:206159378-206159681 | Common:3; Rare:100; Clinvar (benign):1 | ||||
chr2:206765276-206765661 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165937-207166134 | Rare:37 | ||||
chr2:207529695-207530100 | Common:3; Rare:120 | ||||
chr2:208254991-208255234 | Common:2; Rare:62 | ||||
chr2:208266040-208266268 | Common:9; Rare:78; Clinvar (benign):2 | ||||
chr2:213284210-213284494 | Rare:93 | ||||
chr2:215138500-215138739 | Common:2; Rare:52 | ||||
chr2:215312011-215312108 | Common:5; Rare:45 | ||||
chr2:216081756-216081920 | Common:1; Rare:57 | ||||
chr2:216412694-216412775 | Rare:10 | ||||
chr2:216498740-216498901 | Common:6; Rare:70 | ||||
chr2:216694579-216694659 | Rare:21 | ||||
chr2:216694683-216694803 | Rare:34 |