chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	35737226	35737227	A	AT	32	GENIC	homozygous	52138076
10	35737616	35737617	T	G	29	GENIC	homozygous	51409628
10	35738065	35738066	G	A	27	GENIC	homozygous	52138078
10	35738295	35738296	C	T	33	GENIC	homozygous	52138080
10	35739153	35739154	A	C	2	GENIC	homozygous	52138082
10	35739518	35739519	G	-	16	GENIC	possibly homozygous	52138084
10	35739520	35739523	GTG	---	17	GENIC	possibly homozygous	51409638
10	35739650	35739651	T	A	31	GENIC	homozygous	52138086
10	35739677	35739678	C	T	26	GENIC	homozygous	52138088
10	35739915	35739916	T	C	39	GENIC	homozygous	51409644
10	35740118	35740119	A	G	22	GENIC	homozygous	52138090
10	35740439	35740440	A	T	14	GENIC	homozygous	52138092
10	35740665	35740666	C	T	21	GENIC	homozygous	52138094
10	35740841	35740842	A	G	31	GENIC	homozygous	51409646
10	35740955	35740956	A	AG	17	GENIC	homozygous	52138096
10	35740971	35740982	GGGACATGGGT	-----------	23	GENIC	homozygous	52138098
10	35741053	35741054	C	T	12	GENIC	homozygous	52138100
10	35741189	35741190	G	A	23	GENIC	homozygous	52138102
10	35741196	35741197	T	A	22	GENIC	homozygous	52138104
10	35741554	35741555	A	G	35	GENIC	homozygous	52138106
10	35741880	35741881	C	CG	13	GENIC	homozygous	51847513
10	35741923	35741924	G	GA	26	GENIC	homozygous	52138108
10	35741980	35741981	T	C	19	GENIC	homozygous	52138110
10	35742675	35742684	TGTGGGGCT	---------	15	GENIC	homozygous	52138112
10	35743047	35743048	A	T	23	GENIC	homozygous	52138114