chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	93889894	93889895	A	C	32	GENIC	homozygous	51745626
10	93890323	93890324	G	T	39	GENIC	homozygous	52510443
10	93890990	93890991	A	G	34	GENIC	homozygous	52510445
10	93891511	93891512	C	A	40	GENIC	homozygous	52510447
10	93891563	93891564	G	A	29	GENIC	homozygous	52510449
10	93893029	93893030	C	T	41	GENIC	homozygous	52510451
10	93893619	93893620	C	-	31	GENIC	homozygous	51547625
10	93893624	93893625	A	AC	33	GENIC	homozygous	51547626
10	93893740	93893741	A	G	32	GENIC	homozygous	51745630
10	93894474	93894475	A	G	23	GENIC	homozygous	51745634
10	93895306	93895307	C	CTT	8	GENIC	heterozygous	51547627
10	93895306	93895307	C	CTTT	8	GENIC	possibly homozygous	52398895
10	93895741	93895742	T	C	32	GENIC	homozygous	51547628
10	93895906	93895907	C	A	33	GENIC	homozygous	52510453
10	93896266	93896268	CC	--	30	GENIC	homozygous	51547629