Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43546331-43546650 | Common:1; Rare:76 | ||||
chr17:44070633-44070947 | Common:3; Rare:111; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44503378-44503710 | Rare:132 | ||||
chr17:44899375-44899769 | Common:3; Rare:125; Clinvar:3; Clinvar (benign):1 | ||||
chr17:45060993-45061339 | Common:2; Rare:91 | ||||
chr17:47189246-47189616 | Rare:95 | ||||
chr17:47831512-47831610 | Rare:29 | ||||
chr17:47941381-47941726 | Rare:98; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048069-48048366 | Rare:72 | ||||
chr17:48048548-48048791 | Common:3; Rare:49 | ||||
chr17:48610576-48610673 | Rare:29 | ||||
chr17:48944781-48944949 | Common:2; Rare:53 | ||||
chr17:48996975-48997159 | Rare:47 | ||||
chr17:50345956-50346131 | Common:3; Rare:54 | ||||
chr17:50373168-50373261 | Common:3; Rare:39 |