chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 250785784 250785785 G C 31 GENIC homozygous 110850867 2 250786138 250786139 G C 17 GENIC possibly homozygous 110850869 2 250786143 250786144 C G 19 GENIC possibly homozygous 110850871 2 250793057 250793058 C G 62 GENIC homozygous 110850873 2 250793920 250793921 A T 38 GENIC homozygous 110379840 2 250794211 250794212 C T 40 GENIC homozygous 110850874 2 250794497 250794498 A G 43 GENIC heterozygous 110379844 2 250794969 250794970 A G 11 GENIC homozygous 110379846 2 250795651 250795652 C T 44 GENIC homozygous 110850876 2 250796670 250796671 G A 33 GENIC homozygous 110850878 2 250798466 250798467 T A 37 GENIC possibly homozygous 110379856 2 250800397 250800398 G A 39 GENIC homozygous 110850880 2 250800721 250800722 A T 49 GENIC homozygous 110379860 2 250800778 250800779 G A 35 GENIC homozygous 110850882 2 250800794 250800795 G C 40 GENIC homozygous 110850884 2 250800812 250800813 T A 41 GENIC homozygous 110850886 2 250800857 250800858 A G 46 GENIC possibly homozygous 111035702 2 250800872 250800873 C A 49 GENIC homozygous 110850888 2 250800875 250800876 G C 49 GENIC homozygous 110850890 2 250800915 250800916 T C 55 GENIC homozygous 110850892 2 250801069 250801070 C T 40 GENIC heterozygous 110850894 2 250801272 250801273 C T 21 GENIC homozygous 111035704 2 250801298 250801299 C T 31 GENIC heterozygous 110635664 2 250801409 250801410 G A 46 GENIC possibly homozygous 110850895 2 250801489 250801490 A T 33 GENIC homozygous 110850897 2 250801712 250801713 T A 41 GENIC homozygous 110850899 2 250801739 250801740 G A 29 GENIC homozygous 110850901 2 250801884 250801885 C T 47 GENIC possibly homozygous 110850903 2 250801938 250801939 T C 43 GENIC homozygous 110850905 2 250802081 250802082 A G 25 GENIC homozygous 110379861 2 250802357 250802358 A G 62 GENIC homozygous 110850907 2 250802533 250802534 A G 41 GENIC homozygous 110850909 2 250802564 250802565 A C 39 GENIC homozygous 110850911 2 250804353 250804354 A G 53 GENIC homozygous 110379865