chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 10120842 10120843 G A 40 GENIC heterozygous 926300898 12 10133982 10133983 C CTG 38 GENIC heterozygous 926434259 12 10170077 10170078 T C 15 GENIC heterozygous 926300899 12 10173847 10173848 C T 19 GENIC heterozygous 926300900 12 10175884 10175885 T C 54 GENIC heterozygous 926300901 12 10179379 10179380 C T 36 GENIC heterozygous 926300902 12 10188346 10188347 T C 33 GENIC heterozygous 926300903 12 10188931 10188932 A G 47 GENIC heterozygous 926300904 12 10189375 10189376 T C 23 GENIC heterozygous 926300905 12 10189748 10189749 G A 68 GENIC heterozygous 926300906 12 10189793 10189794 T C 66 GENIC heterozygous 926300907 12 10190006 10190007 C T 60 GENIC heterozygous 926300908 12 10190123 10190124 G A 72 GENIC heterozygous 926300909 12 10190180 10190181 T - 65 GENIC heterozygous 926434260 12 10190687 10190688 C T 60 GENIC heterozygous 926300910 12 10190756 10190757 C T 59 GENIC heterozygous 926300911 12 10190912 10190913 T - 98 GENIC heterozygous 926434261 12 10191687 10191688 A G 32 GENIC heterozygous 926300912 12 10191698 10191699 G A 33 GENIC heterozygous 926300913 12 10192497 10192498 T A 42 GENIC heterozygous 926300914 12 10192503 10192504 G C 43 GENIC heterozygous 926300915 12 10192540 10192541 A G 48 GENIC heterozygous 926300916