chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52670885	52670886	A	C	26	GENIC	heterozygous	50230382
13	52671038	52671039	C	G	17	GENIC	possibly homozygous	50230384
13	52671040	52671041	C	G	18	GENIC	possibly homozygous	50230386
13	52671080	52671081	C	G	20	GENIC	homozygous	50040579
13	52672246	52672247	C	T	44	GENIC	homozygous	49948533
13	52673739	52673740	G	A	28	GENIC	homozygous	50230388
13	52673743	52673744	G	A	29	GENIC	homozygous	50230390
13	52675148	52675149	T	C	33	GENIC	homozygous	50230392
13	52675215	52675216	G	A	41	GENIC	homozygous	50230394
13	52675381	52675382	G	A	49	GENIC	homozygous	50230396
13	52678112	52678113	A	AT	17	GENIC	homozygous	49758278
13	52678122	52678123	A	-	15	GENIC	homozygous	49758279
13	52678128	52678129	C	CA	17	GENIC	homozygous	49758280
13	52678149	52678150	A	C	14	GENIC	homozygous	50230398
13	52679788	52679789	C	T	50	GENIC	homozygous	50230400