chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90521372	90521373	G	GC	18	GENIC	homozygous	51538631
10	90521429	90521430	T	TG	2	GENIC	heterozygous	51538632
10	90521429	90521430	T	TGG	2	GENIC	heterozygous	51736875
10	90521475	90521476	G	GC	8	GENIC	homozygous	51538634
10	90521495	90521496	T	TC	14	GENIC	homozygous	51538635
10	90522496	90522497	C	T	33	GENIC	homozygous	51736877
10	90522541	90522542	A	G	44	GENIC	homozygous	51736879
10	90522619	90522620	C	A	30	GENIC	homozygous	51736881
10	90523477	90523478	A	T	45	GENIC	homozygous	51736886
10	90523662	90523663	G	A	25	GENIC	homozygous	51736888
10	90523889	90523890	C	A	35	GENIC	homozygous	51736890
10	90524611	90524612	T	C	25	GENIC	homozygous	51736892
10	90525549	90525550	C	T	28	GENIC	possibly homozygous	52165645
10	90523679	90523680	C	A	24	GENIC	homozygous	52165642
10	90524927	90524928	C	A	26	GENIC	homozygous	52165643
10	90525183	90525184	G	A	29	GENIC	homozygous	52165644
10	90526026	90526034	GTGTGTGT	--------	5	GENIC	homozygous	51736897
10	90529817	90529818	T	C	32	GENIC	homozygous	52165646
10	90530156	90530157	T	TG	18	GENIC	homozygous	52165647
10	90531806	90531807	T	C	31	GENIC	homozygous	51736905
10	90532766	90532767	T	C	32	GENIC	homozygous	51736909
10	90532827	90532828	T	G	40	GENIC	homozygous	51736911
10	90533671	90533672	A	G	9	GENIC	homozygous	52165648
10	90533861	90533862	C	T	32	GENIC	homozygous	52165649
10	90537410	90537411	T	TCC	15	GENIC	homozygous	51538637
10	90529705	90529706	C	T	43	GENIC	homozygous	52206543
10	90537525	90537526	A	T	17	GENIC	homozygous	52206546