chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46326063	46326064	T	TAA	15	GENIC	heterozygous	51444506
10	46326063	46326064	T	TA	15	GENIC	heterozygous	51444507
10	46326318	46326319	G	A	29	GENIC	homozygous	51636802
10	46326461	46326462	C	CAG	39	GENIC	homozygous	51444508
10	46329717	46329718	G	A	23	GENIC	homozygous	51636804
10	46329790	46329791	A	AGGTGGCTCAGC	14	GENIC	homozygous	51444515
10	46329947	46329948	A	-	33	GENIC	homozygous	51636805
10	46330297	46330298	G	T	49	GENIC	homozygous	52154717
10	46332855	46332856	G	A	24	GENIC	homozygous	51636807
10	46332973	46332974	T	G	27	GENIC	homozygous	51444525
10	46333785	46333786	A	G	33	GENIC	homozygous	51444526
10	46334710	46334711	C	T	25	GENIC	heterozygous	52154719
10	46334729	46334730	A	G	25	GENIC	heterozygous	52154721
10	46334752	46334753	G	A	23	GENIC	possibly homozygous	52154723
10	46334756	46334757	T	C	23	GENIC	homozygous	52154725
10	46334793	46334794	T	TTCAC	1	GENIC	homozygous	51444527
10	46335402	46335403	A	ATGTG	12	GENIC	homozygous	51875047
10	46335769	46335770	T	C	36	GENIC	homozygous	51444530
10	46336200	46336202	CC	--	7	GENIC	possibly homozygous	51444532
10	46336211	46336227	TCCGTCCGTCCGTCCG	----------------	4	GENIC	homozygous	51444533
10	46336238	46336239	G	A	13	GENIC	heterozygous	51444534
10	46338748	46338749	T	TACAC	8	GENIC	possibly homozygous	51444540
10	46338903	46338904	C	T	26	GENIC	homozygous	51636812
10	46339489	46339490	A	G	22	GENIC	homozygous	51444542
10	46339805	46339806	A	T	16	GENIC	homozygous	51444543
10	46340825	46340826	C	T	28	GENIC	homozygous	52154727
10	46341435	46341436	T	C	26	GENIC	homozygous	51444547
10	46343272	46343273	G	A	16	GENIC	homozygous	51636815
10	46346409	46346410	T	C	33	GENIC	homozygous	52154729