Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:41031315-41031487 | Rare:39 | ||||
chr1:41165021-41165053 | Rare:6 | ||||
chr1:42317445-42317507 | Rare:11 | ||||
chr1:42696022-42696204 | Rare:39 | ||||
chr1:42920825-42920996 | Rare:29 | ||||
chr1:42928927-42929399 | Common:4; Rare:114; Clinvar:10; Clinvar (benign):19; Clinvar (pathogenic):2 | ||||
chr1:42929576-42930046 | Common:2; Rare:120; Clinvar:9; Clinvar (benign):19; Clinvar (pathogenic):6 | ||||
chr1:42939980-42940243 | Common:1; Rare:39 | ||||
chr1:42940252-42940638 | Common:3; Rare:70 | ||||
chr1:42963626-42963902 | Common:4; Rare:33 | ||||
chr1:42967158-42967444 | Common:6; Rare:42 | ||||
chr1:43411730-43411745 | Rare:1 | ||||
chr1:43448470-43448728 | Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr1:43523175-43523389 | Rare:36 | ||||
chr1:43588892-43589184 | Rare:70 |