chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39849850	39849851	T	C	11	GENIC	homozygous	52963266
8	39850355	39850356	G	A	11	GENIC	homozygous	52963267
8	39851225	39851226	T	-	14	GENIC	homozygous	52963268
8	39851365	39851366	A	AC	11	GENIC	homozygous	52963269
8	39852147	39852148	A	G	11	GENIC	homozygous	52963270
8	39853196	39853197	G	GT	9	GENIC	homozygous	52591826
8	39853617	39853618	C	A	10	GENIC	homozygous	52591827
8	39854010	39854011	T	TGTGG	11	GENIC	homozygous	52963273
8	39854048	39854049	T	C	16	GENIC	homozygous	52963275
8	39854493	39854494	A	AG	15	GENIC	homozygous	52591830
8	39854589	39854591	CA	--	10	GENIC	homozygous	54324521
8	39854668	39854669	A	G	10	GENIC	homozygous	52963277
8	39855820	39855821	T	TTTA	11	GENIC	homozygous	52591832
8	39859141	39859142	G	A	17	GENIC	homozygous	52963278
8	39861533	39861534	G	A	14	GENIC	homozygous	52963280
8	39861797	39861798	C	T	18	GENIC	homozygous	52591833
8	39861972	39861973	C	A	18	GENIC	homozygous	52963281
8	39862331	39862332	T	C	14	GENIC	homozygous	52963282
8	39862564	39862565	T	C	14	GENIC	homozygous	52591835
8	39865529	39865530	G	C	16	GENIC	homozygous	52591858
8	39866815	39866816	C	G	8	GENIC	homozygous	52963295