chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	70486230	70486231	G	A	17	GENIC	homozygous	148081643
11	70486489	70486490	C	T	30	GENIC	homozygous	148081644
11	70486633	70486634	C	T	24	GENIC	homozygous	148081645
11	70487304	70487305	C	T	20	GENIC	homozygous	148081646
11	70486301	70486302	C		7	GENIC	possibly homozygous	148067650
11	70487443	70487451	AAAAATAG		33	GENIC	homozygous	148067651
11	70487175	70487176	T	G	25	GENIC	homozygous	143509691
11	70488049	70488050	A	G	32	GENIC	homozygous	143509693
11	70489834	70489835	C	T	31	GENIC	homozygous	148081647
11	70490400	70490401	G	C	24	GENIC	homozygous	143509699
11	70491089	70491090	T	C	26	GENIC	homozygous	143509703
11	70491195	70491196	T	C	23	GENIC	homozygous	143509704
11	70491355	70491356	A	G	28	GENIC	homozygous	143509706
11	70491356	70491357	T	A	28	GENIC	homozygous	144901815
11	70491817	70491823	GTGGGG		9	GENIC	homozygous	144881162
11	70493736	70493737	C	T	18	GENIC	homozygous	148081648
11	70493835	70493836	A	G	29	GENIC	homozygous	148081649
11	70494051	70494052	C	T	27	GENIC	homozygous	148081650
11	70494746	70494747	T	A	26	GENIC	homozygous	148081651
11	70495806	70495807	C	T	31	GENIC	homozygous	148081652
11	70495911	70495912	A	C	27	GENIC	possibly homozygous	143509717
11	70494456	70494457	G	A	19	GENIC	homozygous	148558100