chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49219805	49219806	A	C	6	GENIC	heterozygous	52971548
8	49221302	49221303	A	AT	2	GENIC	homozygous	52971549
8	49221797	49221798	C	G	6	GENIC	heterozygous	52971551
8	49223053	49223054	G	A	21	GENIC	possibly homozygous	52971555
8	49223593	49223594	G	T	19	GENIC	possibly homozygous	52971556
8	49223666	49223667	A	T	18	GENIC	homozygous	52971557
8	49223883	49223884	T	C	18	GENIC	homozygous	52971558
8	49224347	49224348	A	-	6	GENIC	homozygous	52971559
8	49224597	49224598	C	T	21	GENIC	possibly homozygous	52971560
8	49224681	49224682	T	A	19	GENIC	homozygous	52971561
8	49224767	49224768	G	A	6	GENIC	homozygous	52971562
8	49224953	49224954	C	T	13	GENIC	homozygous	52971563
8	49224991	49224992	G	A	17	GENIC	possibly homozygous	52971564
8	49225026	49225027	T	C	14	GENIC	homozygous	52971565
8	49226155	49226156	G	T	21	GENIC	possibly homozygous	52971567
8	49226175	49226176	G	GGA	13	GENIC	possibly homozygous	52971568
8	49226526	49226527	A	G	22	GENIC	possibly homozygous	52971569
8	49226557	49226558	G	A	16	GENIC	homozygous	52971570
8	49226631	49226632	C	T	17	GENIC	possibly homozygous	52971571
8	49227370	49227371	G	A	13	GENIC	homozygous	52971572
8	49228176	49228177	C	T	3	GENIC	homozygous	52971575
8	49228282	49228283	C	G	18	GENIC	homozygous	52971580
8	49228351	49228352	T	C	13	GENIC	homozygous	52971581
8	49228452	49228453	G	A	20	GENIC	possibly homozygous	52971582
8	49228895	49228896	C	A	19	GENIC	homozygous	52971583
8	49229732	49229733	A	C	17	GENIC	heterozygous	52971586
8	49229998	49229999	T	C	12	GENIC	homozygous	52971587
8	49231081	49231082	A	G	3	GENIC	heterozygous	52971591