chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	93943980	93943981	G	A	15	GENIC	possibly homozygous	52510522
10	93944378	93944379	T	C	7	GENIC	possibly homozygous	51547738
10	93944481	93944482	A	G	3	GENIC	homozygous	51547739
10	93944486	93944487	C	T	3	GENIC	homozygous	52510524
10	93944522	93944523	A	T	4	GENIC	heterozygous	51547740
10	93944528	93944529	T	TCC	3	GENIC	heterozygous	51547741
10	93944913	93944914	A	G	17	GENIC	heterozygous	51547742
10	93945477	93945478	C	-	10	GENIC	heterozygous	51547743
10	93945606	93945607	C	G	16	GENIC	homozygous	51547744
10	93945865	93945866	G	A	13	GENIC	possibly homozygous	51547745
10	93946433	93946434	T	C	10	GENIC	homozygous	51547747
10	93946529	93946530	G	A	12	GENIC	possibly homozygous	52510526
10	93946995	93946996	G	A	20	GENIC	possibly homozygous	51547750
10	93948049	93948051	CC	--	2	GENIC	heterozygous	51745716
10	93948756	93948762	TTGTTG	------	5	GENIC	heterozygous	52510528
10	93949024	93949025	T	C	5	GENIC	homozygous	51547768
10	93949028	93949029	G	-	3	GENIC	homozygous	52510530
10	93949032	93949033	G	GA	2	GENIC	homozygous	51547769
10	93949290	93949295	CCTGT	-----	4	GENIC	heterozygous	52510536
10	93949523	93949524	A	G	7	GENIC	heterozygous	52510538
10	93949897	93949898	C	T	10	GENIC	homozygous	51547778
10	93949939	93949940	G	GCA	7	GENIC	homozygous	51547779
10	93950405	93950406	T	C	16	GENIC	possibly homozygous	51745740
10	93950874	93950875	T	C	16	GENIC	homozygous	51547781
10	93951254	93951258	ACAA	----	9	GENIC	heterozygous	51547793
10	93951289	93951290	C	CACAT	4	GENIC	homozygous	51547796
10	93951308	93951309	T	C	6	GENIC	homozygous	52510550
10	93951890	93951891	A	AAGG	2	GENIC	homozygous	51547797
10	93952657	93952658	T	-	4	GENIC	heterozygous	51547798
10	93952703	93952704	T	C	5	GENIC	heterozygous	51547799
10	93952745	93952746	G	A	3	GENIC	homozygous	52510552
10	93953291	93953292	C	A	21	GENIC	possibly homozygous	52510554
10	93954545	93954546	T	G	3	GENIC	homozygous	51547803
10	93954557	93954558	A	G	4	GENIC	homozygous	51547804
10	93956104	93956105	C	T	19	GENIC	heterozygous	52510558