chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 9552033 9552034 C T 34 GENIC homozygous 814139789 17 9552155 9552156 T C 40 GENIC homozygous 814139790 17 9553146 9553147 A G 32 GENIC homozygous 814139791 17 9553389 9553390 T C 30 GENIC homozygous 814139792 17 9553939 9553940 G A 55 GENIC heterozygous 814139793 17 9553948 9553949 G A 57 GENIC heterozygous 814139794 17 9553960 9553961 A G 48 GENIC heterozygous 814139795 17 9553976 9553977 G A 43 GENIC heterozygous 814139796 17 9554075 9554076 T G 22 GENIC homozygous 814139797 17 9555004 9555005 G T 29 GENIC homozygous 814139798 17 9555084 9555085 T A 35 GENIC homozygous 814139799 17 9556236 9556237 A G 31 GENIC homozygous 814139800 17 9556553 9556554 C T 19 GENIC homozygous 814139801 17 9557398 9557399 G A 20 GENIC homozygous 814139802 17 9557437 9557438 C A 17 GENIC homozygous 814139803 17 9557955 9557956 G A 31 GENIC homozygous 814139804 17 9557959 9557960 G A 33 GENIC homozygous 814139805 17 9558576 9558577 T C 27 GENIC homozygous 814139806