chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	93944322	93944323	C	A	21	GENIC	homozygous	53166495
10	93944528	93944529	T	TCC	4	GENIC	heterozygous	51547741
10	93945900	93945901	G	A	17	GENIC	possibly homozygous	53166497
10	93946433	93946434	T	C	17	GENIC	homozygous	51547747
10	93946995	93946996	G	A	18	GENIC	homozygous	51547750
10	93947029	93947030	C	A	10	GENIC	heterozygous	53166499
10	93949616	93949617	C	T	7	GENIC	homozygous	51547777
10	93949631	93949632	A	T	5	GENIC	heterozygous	53166509
10	93949897	93949898	C	T	16	GENIC	possibly homozygous	51547778
10	93949939	93949940	G	GCA	12	GENIC	homozygous	51547779
10	93950262	93950263	T	TGTTTGTTTGTTTGTTTG	6	GENIC	heterozygous	53166513
10	93950405	93950406	T	C	21	GENIC	homozygous	51745740
10	93951205	93951215	ACACACACAG	----------	3	GENIC	homozygous	51547789
10	93951289	93951290	C	CACAT	5	GENIC	heterozygous	51547796
10	93951890	93951891	A	AAGGAGG	2	GENIC	homozygous	53166517
10	93951940	93951941	G	A	9	GENIC	homozygous	51745746
10	93952276	93952277	G	A	16	GENIC	possibly homozygous	51745748
10	93952609	93952610	C	-	13	GENIC	homozygous	51745750
10	93952657	93952658	T	-	5	GENIC	homozygous	51547798
10	93952703	93952704	T	C	9	GENIC	homozygous	51547799
10	93952960	93952961	T	C	8	GENIC	possibly homozygous	51745752
10	93952990	93952991	G	GA	3	GENIC	heterozygous	51745754
10	93953121	93953122	C	T	14	GENIC	homozygous	51745756
10	93953256	93953271	TATATGGCCTTTAAG	---------------	1	GENIC	homozygous	53166519
10	93954089	93954090	G	A	19	GENIC	possibly homozygous	53166521
10	93954545	93954546	T	G	1	GENIC	homozygous	51547803
10	93954557	93954558	A	G	1	GENIC	homozygous	51547804