chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	145990094	145990095	C	T	10	GENIC	homozygous	185935878
3	145992861	145992862	G	C	14	GENIC	homozygous	185935879
3	145994669	145994670	T	C	24	GENIC	homozygous	185935880
3	145995092	145995093	T	C	6	GENIC	homozygous	185935881
3	145996179	145996180	C	T	28	GENIC	possibly homozygous	185935882
3	145996261	145996262	A	G	20	GENIC	possibly homozygous	185935883
3	145996773	145996774	C	A	11	GENIC	homozygous	185935884
3	145996797	145996798	T	G	10	GENIC	homozygous	185095360
3	145997072	145997073	C	T	16	GENIC	homozygous	185935885
3	145999084	145999085	A	G	20	GENIC	homozygous	185095361
3	145999493	145999494	G	A	17	GENIC	homozygous	185935886
3	145999607	145999608	T	A	13	GENIC	homozygous	185935887
3	145999729	145999730	G	A	12	GENIC	homozygous	185935888
3	145999790	145999791	A	G	9	GENIC	possibly homozygous	185935889
3	146000602	146000603	G	A	9	GENIC	homozygous	185935890
3	146002355	146002356	G	A	21	GENIC	possibly homozygous	185935891
3	146002592	146002593	T	C	7	GENIC	homozygous	185935892
3	146002846	146002847	T	C	11	GENIC	homozygous	185935893
3	146003877	146003878	A	G	16	GENIC	homozygous	185095362
3	146004144	146004145	G	A	13	GENIC	possibly homozygous	185935894
3	146004566	146004567	A	G	14	GENIC	homozygous	185095363
3	146005893	146005894	A	G	15	GENIC	homozygous	185935895
3	146006011	146006012	T	C	10	GENIC	homozygous	185935896
3	146006230	146006231	A	C	20	GENIC	homozygous	185935897
3	146006421	146006422	A	G	18	GENIC	homozygous	185095364
3	146006862	146006863	G	A	21	GENIC	homozygous	185935898
3	146007272	146007273	C	T	9	GENIC	homozygous	185935899
3	146007333	146007334	C	A	18	GENIC	homozygous	185935900
3	146007634	146007635	G	A	19	GENIC	homozygous	185935901
3	146008630	146008631	A	T	18	GENIC	homozygous	185935902