chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 32295683 32295684 T A 30 GENIC homozygous 554630132 16 32295691 32295692 A T 32 GENIC homozygous 554630133 16 32295700 32295701 A - 33 GENIC homozygous 702026852 16 32295701 32295702 T C 33 GENIC homozygous 554630134 16 32295706 32295707 T A 33 GENIC homozygous 554630135 16 32295713 32295714 T A 30 GENIC homozygous 554630136 16 32295715 32295716 G C 32 GENIC homozygous 554630137 16 32295718 32295719 T C 30 GENIC homozygous 554630138 16 32296112 32296113 G GTGCTTGCTAGGCA 5 GENIC homozygous 702026853 16 32296116 32296117 G GCTCTACCACTGAGCTAA 5 GENIC homozygous 702026854 16 32296121 32296122 T C 4 GENIC homozygous 554630139 16 32296205 32296207 TG -- 6 GENIC heterozygous 702026855 16 32305842 32305843 T C 20 GENIC homozygous 554630140 16 32321104 32321108 TCTA ---- 9 GENIC homozygous 702026857 16 32326864 32326865 G - 4 GENIC homozygous 702026860 16 32343584 32343585 T TG 9 GENIC homozygous 702026862