chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	93716963	93716964	G	A	12	GENIC	possibly homozygous	49965839
13	93717849	93717850	A	AG	15	GENIC	possibly homozygous	49965840
13	93718124	93718125	G	A	14	GENIC	possibly homozygous	50982768
13	93718514	93718515	T	C	4	GENIC	heterozygous	50838220
13	93718600	93718601	T	C	5	GENIC	homozygous	49965841
13	93718970	93718971	C	T	9	GENIC	homozygous	49965842
13	93719089	93719090	T	C	16	GENIC	homozygous	50982770
13	93719224	93719225	T	C	17	GENIC	homozygous	50982771
13	93719538	93719539	G	A	16	GENIC	homozygous	49965844
13	93719878	93719879	G	GC	13	GENIC	homozygous	49965845
13	93719879	93719880	T	C	13	GENIC	homozygous	50497465
13	93719991	93719992	T	C	12	GENIC	heterozygous	49965846
13	93723028	93723029	T	C	12	GENIC	homozygous	50982772
13	93723180	93723181	C	G	15	GENIC	possibly homozygous	50982773
13	93723379	93723380	A	C	4	GENIC	homozygous	49965848
13	93723670	93723671	T	G	9	GENIC	homozygous	50982774
13	93723872	93723873	G	C	11	GENIC	possibly homozygous	49965852
13	93730110	93730111	A	T	2	GENIC	heterozygous	49965867
13	93730111	93730112	A	T	2	GENIC	heterozygous	50982775
13	93730597	93730598	T	G	26	GENIC	possibly homozygous	50982776
13	93730652	93730653	T	C	16	GENIC	homozygous	49965868
13	93730989	93730990	G	C	9	GENIC	possibly homozygous	49965869
13	93731202	93731203	C	CA	14	GENIC	possibly homozygous	50982777
13	93734325	93734326	C	A	11	GENIC	heterozygous	50982778
13	93734393	93734394	C	T	14	GENIC	homozygous	49965872
13	93734659	93734660	T	C	16	GENIC	possibly homozygous	49965873
13	93735724	93735725	T	TCTGG	6	GENIC	heterozygous	49965875
13	93736412	93736413	A	G	1	GENIC	homozygous	50497466