chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 183733749 183733750 A G 29 GENIC homozygous 108442933 1 183733973 183733974 G A 21 GENIC homozygous 108442935 1 183734050 183734051 T 28 GENIC homozygous 127462096 1 183734692 183734693 T C 23 GENIC homozygous 108442937 1 183734739 183734740 T C 24 GENIC homozygous 108442939 1 183735704 183735705 G A 17 GENIC possibly homozygous 108442941 1 183736851 183736852 T C 24 GENIC homozygous 108442943 1 183736969 183736970 A G 17 GENIC homozygous 108442945 1 183737389 183737390 A G 32 GENIC homozygous 108442947 1 183738671 183738672 T C 26 GENIC homozygous 108442949 1 183738760 183738761 C T 27 GENIC homozygous 108442951 1 183739090 183739091 A 18 GENIC possibly homozygous 127462097 1 183739776 183739777 A G 22 GENIC homozygous 108442953 1 183741701 183741702 G A 20 GENIC homozygous 108442955 1 183741995 183741996 T C 10 GENIC homozygous 108442957 1 183742233 183742234 A C 13 GENIC homozygous 108442959 1 183743163 183743164 T C 30 GENIC homozygous 108442961 1 183743752 183743753 T C 16 GENIC homozygous 108442963 1 183743929 183743930 C G 23 GENIC homozygous 108442965 1 183744306 183744307 C A 15 GENIC homozygous 108442967