chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	70486295	70486295		GGT	9	GENIC	homozygous	144881158
11	70486620	70486621	G	A	32	GENIC	homozygous	144901805
11	70486677	70486678	C	T	28	GENIC	homozygous	144901806
11	70486886	70486887	G	A	35	GENIC	homozygous	144901807
11	70487175	70487176	T	G	43	GENIC	homozygous	143509691
11	70487539	70487540	A	T	27	GENIC	possibly homozygous	144901808
11	70487573	70487574	T	G	19	GENIC	homozygous	144901809
11	70487582	70487582		A	19	GENIC	homozygous	143478843
11	70487819	70487820	G	A	36	GENIC	homozygous	144901810
11	70488049	70488050	A	G	35	GENIC	homozygous	143509693
11	70488148	70488155	TGCATGC		26	GENIC	homozygous	144881159
11	70488300	70488308	TGTGTGCA		30	GENIC	homozygous	144881160
11	70488590	70488591	A	G	18	GENIC	homozygous	144901811
11	70488958	70488959	G	C	41	GENIC	homozygous	143509694
11	70489010	70489011	G	A	34	GENIC	homozygous	144901812
11	70489028	70489029	T		34	GENIC	homozygous	144881161
11	70490400	70490401	G	C	44	GENIC	homozygous	143509699
11	70490574	70490575	G	T	28	GENIC	homozygous	144901813
11	70490629	70490630	T	C	38	GENIC	homozygous	143509700
11	70490807	70490808	C	T	44	GENIC	homozygous	143509702
11	70491089	70491090	T	C	41	GENIC	homozygous	143509703
11	70491195	70491196	T	C	57	GENIC	possibly homozygous	143509704
11	70491249	70491250	C	A	59	GENIC	possibly homozygous	144901814
11	70491355	70491356	A	G	38	GENIC	homozygous	143509706
11	70491356	70491357	T	A	39	GENIC	homozygous	144901815
11	70491639	70491640	C	T	45	GENIC	homozygous	144901816
11	70491817	70491823	GTGGGG		7	GENIC	homozygous	144881162
11	70492031	70492032	T	C	27	GENIC	homozygous	144901817
11	70492320	70492321	G	C	27	GENIC	homozygous	144901818
11	70492573	70492574	C	G	13	GENIC	homozygous	144901819
11	70495506	70495507	T	C	36	GENIC	homozygous	143509713
11	70495595	70495596	A	G	36	GENIC	homozygous	143509714
11	70495762	70495763	C	T	31	GENIC	homozygous	143509716
11	70495911	70495912	A	C	39	GENIC	homozygous	143509717