chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 157791822 157791823 T C 34 GENIC homozygous 775118850 4 157791833 157791834 T C 30 GENIC possibly homozygous 775118851 4 157791845 157791846 T A 38 GENIC possibly homozygous 775118852 4 157791851 157791852 T C 39 GENIC possibly homozygous 775118853 4 157791863 157791864 A T 41 GENIC heterozygous 775118854 4 157792271 157792272 G A 49 GENIC homozygous 775118855 4 157793017 157793018 G T 59 GENIC possibly homozygous 775118856 4 157795166 157795167 C T 27 GENIC homozygous 775118857 4 157796662 157796663 T C 54 GENIC homozygous 775118858 4 157796750 157796751 C T 36 GENIC homozygous 775118859 4 157797124 157797125 G A 55 GENIC homozygous 775118860 4 157797798 157797799 G T 23 GENIC heterozygous 775118861 4 157797801 157797802 C T 23 GENIC heterozygous 775118862 4 157797854 157797855 T G 31 GENIC homozygous 775118863 4 157798356 157798357 T G 56 GENIC homozygous 775118864