chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	203606085	203606086	A	G	27	GENIC	homozygous	75281759
2	203606863	203606864	G	T	14	GENIC	homozygous	75281761
2	203606988	203606989	G	T	23	GENIC	homozygous	75281763
2	203607404	203607405	A	G	33	GENIC	homozygous	74284211
2	203607742	203607743	C	T	25	GENIC	homozygous	75087131
2	203608201	203608202	A	C	28	GENIC	possibly homozygous	75281765
2	203608993	203608994	G	A	27	GENIC	homozygous	75281767
2	203609063	203609064	A	G	30	GENIC	possibly homozygous	75281769
2	203609086	203609087	G	C	27	GENIC	homozygous	75281771
2	203609164	203609165	A	G	27	GENIC	homozygous	75281773
2	203609850	203609851	C	T	28	GENIC	homozygous	75281775
2	203609862	203609863	A	G	28	GENIC	homozygous	74284229
2	203609897	203609898	C	T	25	GENIC	homozygous	75281777
2	203610104	203610105	A	G	34	GENIC	homozygous	74284232
2	203610234	203610235	A	T	27	GENIC	homozygous	74284235
2	203610257	203610258	C	T	19	GENIC	homozygous	75281779
2	203610285	203610286	T	A	23	GENIC	heterozygous	75281781
2	203610675	203610676	A	G	18	GENIC	homozygous	75281783