Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45013905-45014470 | Common:10; Rare:215; Clinvar (benign):2; Clinvar (pathogenic):8 | ||||
chr1:45206352-45206518 | Common:1; Rare:59 | ||||
chr1:45206520-45206870 | Common:1; Rare:102 | ||||
chr1:45339425-45339825 | Common:1; Rare:138 | ||||
chr1:45339781-45340285 | Common:11; Rare:1074; Clinvar:57; Clinvar (benign):40; Clinvar (pathogenic):6 | ||||
chr1:45340301-45340701 | Common:11; Rare:401; Clinvar:11; Clinvar (benign):4 | ||||
chr1:45340913-45341632 | Common:4; Rare:349; Clinvar (pathogenic):2 | ||||
chr1:45491024-45491424 | Common:8; Rare:226 | ||||
chr1:45499371-45500742 | Common:16; Rare:957; Clinvar:34; Clinvar (pathogenic):27 | ||||
chr1:45521610-45522286 | Common:10; Rare:891 | ||||
chr1:45522323-45522890 | Common:5; Rare:183 | ||||
chr1:45550450-45551300 | Common:25; Rare:805 | ||||
chr1:45583198-45584920 | Common:25; Rare:1594 | ||||
chr1:45685763-45686217 | Common:2; Rare:174 | ||||
chr1:45686330-45686780 | Rare:627 |