Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45011871-45012293 | Common:5; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45339585-45339729 | Rare:26 | ||||
chr1:45339996-45340041 | Rare:12 | ||||
chr1:45340109-45340182 | Rare:27 | ||||
chr1:45340233-45340523 | Common:2; Rare:95; Clinvar:12; Clinvar (benign):3 | ||||
chr1:45491156-45491416 | Common:1; Rare:64 | ||||
chr1:45500005-45500369 | Common:2; Rare:87; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521845-45521975 | Common:1; Rare:54 | ||||
chr1:45550704-45551097 | Common:3; Rare:98 | ||||
chr1:45583912-45584212 | Common:1; Rare:114 | ||||
chr1:45686474-45686680 | Rare:78 | ||||
chr1:45687036-45687390 | Common:2; Rare:95 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:45803507-45803612 | Common:1; Rare:34 | ||||
chr1:46131755-46132367 | Common:2; Rare:163 |