chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 38105003 38105004 C T 36 GENIC heterozygous 530163309 8 38105020 38105021 A T 35 GENIC heterozygous 532560110 8 38105063 38105064 A G 44 GENIC heterozygous 532560111 8 38105069 38105070 T A 40 GENIC heterozygous 532560112 8 38105095 38105096 C T 43 GENIC heterozygous 532560113 8 38105105 38105106 T C 46 GENIC heterozygous 532560114 8 38105109 38105110 A C 46 GENIC heterozygous 532560115 8 38105173 38105174 G A 42 GENIC heterozygous 532560116 8 38105372 38105373 T C 53 GENIC heterozygous 532560117 8 38105377 38105378 A G 55 GENIC heterozygous 532560118 8 38105389 38105390 T C 54 GENIC heterozygous 532560119 8 38105466 38105467 C G 56 GENIC heterozygous 532560120 8 38105479 38105480 G A 53 GENIC heterozygous 532560121 8 38105487 38105488 G A 58 GENIC heterozygous 532560122 8 38105523 38105524 G T 59 GENIC heterozygous 532560123 8 38105697 38105698 G C 31 GENIC heterozygous 532560124 8 38105718 38105719 T G 21 GENIC heterozygous 532560125 8 38105722 38105723 A G 21 GENIC heterozygous 532560126 8 38105730 38105731 C T 22 GENIC heterozygous 532560127 8 38105751 38105752 A C 21 GENIC heterozygous 532560128 8 38105753 38105754 T G 22 GENIC heterozygous 532560129 8 38105759 38105760 A G 24 GENIC heterozygous 532560130 8 38105981 38105982 C T 36 GENIC heterozygous 532560131 8 38105996 38105997 C T 24 GENIC heterozygous 532560132