chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 109216387 109216389 GT -- 20 GENIC homozygous 817254707 6 109216449 109216450 A C 26 GENIC homozygous 817254708 6 109216711 109216712 C G 31 GENIC homozygous 817254709 6 109217708 109217709 G A 14 GENIC homozygous 817254710 6 109218078 109218079 T G 14 GENIC homozygous 817254711 6 109218132 109218133 G A 14 GENIC homozygous 817254712 6 109218533 109218534 T C 12 GENIC homozygous 817254713 6 109218971 109218972 C G 14 GENIC homozygous 817254714 6 109219945 109219946 G A 12 GENIC homozygous 817254715 6 109220171 109220172 A G 10 GENIC homozygous 817254716 6 109221479 109221480 A G 16 GENIC homozygous 817254717 6 109224251 109224252 C T 14 GENIC homozygous 817254718 6 109224503 109224504 C T 16 GENIC homozygous 817254719 6 109225632 109225633 T C 19 GENIC homozygous 817254720 6 109225969 109225970 G C 14 GENIC homozygous 817254721 6 109226303 109226304 G - 12 GENIC homozygous 817254722 6 109226869 109226870 T - 13 GENIC homozygous 817254723 6 109227067 109227069 GA -- 8 GENIC homozygous 817254724 6 109227384 109227385 T C 18 GENIC homozygous 817254725 6 109227512 109227513 T A 10 GENIC homozygous 817254726 6 109228010 109228011 G A 17 GENIC homozygous 817254727