Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42577645-42577864 | Common:1; Rare:107 | ||||
chr17:42609333-42609711 | Common:8; Rare:155; Clinvar (benign):1 | ||||
chr17:42833340-42833497 | Rare:59 | ||||
chr17:43171043-43171245 | Rare:61 | ||||
chr17:44070611-44070925 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186701-44186998 | Rare:96 | ||||
chr17:44324780-44324982 | Common:2; Rare:71 | ||||
chr17:44345072-44345321 | Rare:52; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44503377-44503713 | Rare:132 | ||||
chr17:44899379-44899461 | Rare:36 | ||||
chr17:45060987-45061339 | Common:2; Rare:93 | ||||
chr17:46225359-46225496 | Common:2; Rare:39 | ||||
chr17:46922880-46923179 | Common:2; Rare:82; Clinvar (benign):6 | ||||
chr17:47189235-47189591 | Rare:90 | ||||
chr17:47941387-47941712 | Rare:90; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 |