chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90521475	90521476	G	GC	1	GENIC	homozygous	51538634
10	90521495	90521496	T	TC	1	GENIC	homozygous	51538635
10	90522371	90522374	CGG	---	5	GENIC	homozygous	52396537
10	90522496	90522497	C	T	4	GENIC	homozygous	51736877
10	90522541	90522542	A	G	9	GENIC	homozygous	51736879
10	90522619	90522620	C	A	12	GENIC	homozygous	51736881
10	90523318	90523321	TTG	---	2	GENIC	homozygous	52396539
10	90524611	90524612	T	C	3	GENIC	homozygous	51736892
10	90524927	90524928	C	A	12	GENIC	possibly homozygous	52165643
10	90524989	90524990	C	T	7	GENIC	homozygous	52396541
10	90525183	90525184	G	A	5	GENIC	homozygous	52165644
10	90525956	90525958	TG	--	8	GENIC	homozygous	52396543
10	90529736	90529737	C	T	13	GENIC	possibly homozygous	52396554
10	90531053	90531054	C	T	5	GENIC	heterozygous	52396556
10	90531806	90531807	T	C	7	GENIC	homozygous	51736905
10	90532016	90532017	C	G	6	GENIC	homozygous	52396558
10	90532766	90532767	T	C	1	GENIC	homozygous	51736909
10	90532827	90532828	T	G	3	GENIC	heterozygous	51736911
10	90533671	90533672	A	G	4	GENIC	heterozygous	52165648
10	90533698	90533699	C	T	7	GENIC	homozygous	52396560
10	90535013	90535014	C	T	12	GENIC	possibly homozygous	52396564
10	90536309	90536310	T	C	18	GENIC	possibly homozygous	51736919
10	90538183	90538184	A	C	11	GENIC	possibly homozygous	51736923