Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42458738-42458945 | Common:3; Rare:79 | ||||
chr17:42566940-42567159 | Common:3; Rare:77 | ||||
chr17:42577682-42577844 | Rare:77 | ||||
chr17:42609316-42609723 | Common:8; Rare:171; Clinvar (benign):2 | ||||
chr17:42761075-42761227 | Rare:40 | ||||
chr17:42773364-42773475 | Rare:31 | ||||
chr17:42798668-42798785 | Rare:38 | ||||
chr17:42833364-42833461 | Rare:37 | ||||
chr17:43170297-43170712 | Common:3; Rare:80 | ||||
chr17:43171024-43171251 | Rare:70 | ||||
chr17:43211773-43211890 | Common:1; Rare:25 | ||||
chr17:43398872-43398994 | Common:1; Rare:35 | ||||
chr17:43778922-43779048 | Rare:27 | ||||
chr17:44070612-44070918 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123599-44123849 | Common:3; Rare:71 |