chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	50473533	50473534	T	G	14	GENIC	homozygous	143449532
10	50473753	50473759	GGCCCG		19	GENIC	homozygous	143431425
10	50473937	50473938	C	T	24	GENIC	homozygous	143449533
10	50474239	50474240	C	A	15	GENIC	homozygous	138789549
10	50474648	50474649	T	G	16	GENIC	homozygous	143449534
10	50475543	50475544	T	C	10	GENIC	homozygous	138789554
10	50477252	50477253	T	C	20	GENIC	homozygous	143449535
10	50477481	50477482	T	C	24	GENIC	homozygous	143449536
10	50477367	50477368	T		9	GENIC	homozygous	138683622
10	50477869	50477869		GT	11	GENIC	homozygous	143431426
10	50478110	50478113	CAA		30	GENIC	homozygous	138683624
10	50478337	50478338	C	T	19	GENIC	homozygous	143449537
10	50482494	50482495	T	C	18	GENIC	homozygous	138789568
10	50483512	50483513	T	C	23	GENIC	homozygous	138789575
10	50485073	50485074	A	T	22	GENIC	homozygous	138789577
10	50488790	50488790		A	19	GENIC	homozygous	143431427
10	50488957	50488958	A	G	28	GENIC	homozygous	138789590
10	50489669	50489670	C	T	20	GENIC	homozygous	138789591
10	50490103	50490104	T	C	18	GENIC	homozygous	138789592
10	50490265	50490266	A	T	30	GENIC	homozygous	138789593
10	50490489	50490490	C	T	14	GENIC	possibly homozygous	138789595
10	50484794	50484795	A	G	19	GENIC	homozygous	140904447
10	50490365	50490366	G	A	23	GENIC	homozygous	138789594
10	50491997	50491998	A	G	31	GENIC	homozygous	138789596
10	50492744	50492745	A	G	10	GENIC	homozygous	138789597
10	50493356	50493357	C	G	19	GENIC	homozygous	138789598
10	50493358	50493359	C	A	17	GENIC	homozygous	138789599
10	50495238	50495239	G	C	16	GENIC	homozygous	138789600
10	50495527	50495528	T	C	16	GENIC	homozygous	138789601
10	50490722	50490723	C	A	9	GENIC	heterozygous	404085164
10	50490722	50490723	C		9	GENIC	homozygous	404085165
10	50490716	50490717	C		9	GENIC	homozygous	403733053
10	50490716	50490717	C	A	9	GENIC	heterozygous	403733054