Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:211675811-211676164 | Common:6; Rare:75 | ||||
chr1:211830309-211830383 | Common:1; Rare:20 | ||||
chr1:211830655-211830985 | Common:1; Rare:82 | ||||
chr1:212035494-212035822 | Common:2; Rare:91 | ||||
chr1:212284974-212285637 | Common:6; Rare:186 | ||||
chr1:212285769-212285967 | Common:1; Rare:54 | ||||
chr1:212414705-212415118 | Common:3; Rare:123 | ||||
chr1:212432716-212432985 | Rare:73 | ||||
chr1:212608155-212608513 | Common:4; Rare:79 | ||||
chr1:212608517-212609007 | Common:1; Rare:119 | ||||
chr1:212609191-212609625 | Common:3; Rare:90 | ||||
chr1:212791556-212792392 | Common:9; Rare:261 | ||||
chr1:212857685-212857902 | Common:1; Rare:41 | ||||
chr1:212858040-212858471 | Common:6; Rare:119; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:212950375-212950649 | Common:2; Rare:70 |