chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	103512343	103512344	A	G	6	GENIC	homozygous	52779044
8	103513747	103513748	C	G	24	GENIC	possibly homozygous	52779045
8	103517054	103517055	G	A	9	GENIC	heterozygous	52779046
8	103518156	103518157	G	A	7	GENIC	homozygous	52779049
8	103519323	103519324	C	G	20	GENIC	homozygous	52779050
8	103519399	103519400	G	C	1	GENIC	homozygous	52779051
8	103522024	103522025	A	T	7	GENIC	homozygous	52779054
8	103525126	103525130	AAAC	----	2	GENIC	homozygous	52779057
8	103525391	103525392	C	CTG	8	GENIC	heterozygous	53158050
8	103525860	103525861	A	T	1	GENIC	homozygous	52779059
8	103526248	103526249	T	C	10	GENIC	heterozygous	53158056
8	103531582	103531583	G	A	7	GENIC	homozygous	52779065
8	103534473	103534474	T	TCC	2	GENIC	homozygous	53406369
8	103538569	103538570	A	-	6	GENIC	heterozygous	52779068
8	103539417	103539418	A	G	11	GENIC	possibly homozygous	52779069
8	103543670	103543671	C	T	23	GENIC	possibly homozygous	52779073
8	103545832	103545833	C	T	20	GENIC	homozygous	52779075
8	103548407	103548408	A	G	3	GENIC	homozygous	52779077
8	103549866	103549867	C	T	21	GENIC	possibly homozygous	52779084
8	103552638	103552639	T	-	6	GENIC	homozygous	52779086
8	103552872	103552873	G	A	11	GENIC	heterozygous	52779087
8	103552948	103552949	C	T	8	GENIC	possibly homozygous	52779088
8	103553747	103553748	G	A	10	GENIC	homozygous	52779089