chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 9552033 9552034 C T 41 GENIC possibly homozygous 796155416 17 9552155 9552156 T C 28 GENIC homozygous 796155417 17 9553146 9553147 A G 34 GENIC possibly homozygous 796155418 17 9553389 9553390 T C 42 GENIC homozygous 796155419 17 9553939 9553940 G A 47 GENIC heterozygous 796155420 17 9553948 9553949 G A 49 GENIC heterozygous 796155421 17 9553960 9553961 A G 48 GENIC heterozygous 796155422 17 9553976 9553977 G A 46 GENIC heterozygous 796155423 17 9554075 9554076 T G 46 GENIC possibly homozygous 796155424 17 9554866 9554867 G A 28 GENIC homozygous 796155425 17 9555004 9555005 G T 38 GENIC homozygous 796155426 17 9555084 9555085 T A 39 GENIC homozygous 796155427 17 9556236 9556237 A G 11 GENIC homozygous 796155428 17 9556553 9556554 C T 34 GENIC homozygous 796155429 17 9557398 9557399 G A 53 GENIC homozygous 796155430 17 9557437 9557438 C A 34 GENIC homozygous 796155431 17 9557955 9557956 G A 39 GENIC possibly homozygous 796155432 17 9558576 9558577 T C 21 GENIC homozygous 796155433