Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159923292-159923506 | Rare:48 | ||||
chr1:159923719-159923907 | Common:1; Rare:32 | ||||
chr1:159924554-159924804 | Rare:54 | ||||
chr1:159925456-159925617 | Common:1; Rare:42 | ||||
chr1:160031837-160032166 | Common:3; Rare:87 | ||||
chr1:160098862-160099115 | Common:2; Rare:43 | ||||
chr1:160135940-160136325 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:160211435-160211628 | Common:1; Rare:44 | ||||
chr1:160261664-160261761 | Common:1; Rare:24 | ||||
chr1:160262107-160262202 | Rare:25 | ||||
chr1:160343157-160343403 | Rare:96 | ||||
chr1:160647003-160647058 | Rare:12 | ||||
chr1:161021072-161021244 | Common:5; Rare:56 | ||||
chr1:161038905-161039003 | Rare:39 | ||||
chr1:161045878-161046061 | Common:1; Rare:47 |