Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44324750-44325003 | Common:2; Rare:93 | ||||
chr17:44350506-44350801 | Rare:104; Clinvar:6; Clinvar (benign):4 | ||||
chr17:44352206-44352519 | Common:1; Rare:98; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr17:44503370-44503714 | Rare:134 | ||||
chr17:44899375-44899774 | Common:3; Rare:126; Clinvar:3; Clinvar (benign):1 | ||||
chr17:45051414-45051693 | Common:1; Rare:90 | ||||
chr17:45060987-45061339 | Common:2; Rare:93 | ||||
chr17:45132256-45132656 | Common:3; Rare:125 | ||||
chr17:45148139-45148615 | Common:1; Rare:161 | ||||
chr17:45161555-45161856 | Common:1; Rare:66 | ||||
chr17:45490708-45490863 | Rare:54 | ||||
chr17:46193411-46193613 | Common:3; Rare:55 | ||||
chr17:46922880-46923204 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):8 | ||||
chr17:47188830-47189048 | Common:1; Rare:41 | ||||
chr17:47189111-47189340 | Common:1; Rare:63 |