Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43170965-43171255 | Rare:97 | ||||
chr17:43211747-43211903 | Common:2; Rare:34 | ||||
chr17:43545621-43545778 | Common:1; Rare:45 | ||||
chr17:43778907-43779078 | Rare:40 | ||||
chr17:44070607-44070947 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186629-44187002 | Common:1; Rare:134 | ||||
chr17:44210810-44211127 | Common:1; Rare:93 | ||||
chr17:44324765-44324966 | Common:2; Rare:73 | ||||
chr17:44350795-44351114 | Rare:104; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr17:44503377-44503747 | Rare:141 | ||||
chr17:44899367-44899741 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
chr17:44947664-44947915 | Common:1; Rare:69 | ||||
chr17:45060993-45061358 | Common:2; Rare:104 | ||||
chr17:45148150-45148478 | Common:1; Rare:94 | ||||
chr17:45161530-45161773 | Common:1; Rare:54 |