Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42681565-42682544 | Common:14; Rare:1045 | ||||
chr1:42682732-42683132 | Common:2; Rare:292 | ||||
chr1:42683045-42683473 | Common:3; Rare:326 | ||||
chr1:42766405-42766859 | Common:1; Rare:262; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:42766924-42767377 | Common:33; Rare:855; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr1:42816650-42817801 | Common:11; Rare:1302 | ||||
chr1:42824996-42825839 | Common:3; Rare:430 | ||||
chr1:42846322-42846758 | Common:7; Rare:628 | ||||
chr1:42846808-42847602 | Common:4; Rare:164 | ||||
chr1:42930467-42931323 | Common:1; Rare:278; Clinvar:27; Clinvar (benign):26; Clinvar (pathogenic):1 | ||||
chr1:42952460-42952840 | Rare:68 | ||||
chr1:42957921-42958691 | Common:14; Rare:348; Clinvar (benign):5 | ||||
chr1:42958733-42959360 | Common:32; Rare:695; Clinvar:47; Clinvar (benign):30 | ||||
chr1:43172126-43172393 | Common:6; Rare:314 | ||||
chr1:43172448-43172848 | Common:21; Rare:216 |