chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	51803919	51803920	T	C	21	GENIC	homozygous	52974482
8	51804065	51804066	A	-	7	GENIC	possibly homozygous	52974483
8	51804199	51804200	T	C	5	GENIC	homozygous	52974484
8	51806229	51806230	C	T	21	GENIC	possibly homozygous	52974486
8	51808827	51808828	G	T	23	GENIC	possibly homozygous	52974490
8	51809231	51809232	A	G	14	GENIC	possibly homozygous	52974491
8	51809992	51809993	G	A	4	GENIC	homozygous	52974492
8	51810150	51810151	C	T	30	GENIC	possibly homozygous	52974493
8	51810806	51810807	T	C	19	GENIC	homozygous	52974496
8	51811099	51811101	AA	--	3	GENIC	homozygous	52974497
8	51811121	51811122	C	T	9	GENIC	homozygous	52974498
8	51811347	51811348	A	G	25	GENIC	possibly homozygous	52974499
8	51812446	51812447	G	A	19	GENIC	possibly homozygous	52974500
8	51812830	51812831	A	G	18	GENIC	possibly homozygous	52974501
8	51813973	51813974	A	G	16	GENIC	homozygous	52974502
8	51815164	51815165	C	T	15	GENIC	homozygous	52974504
8	51815667	51815668	G	A	19	GENIC	homozygous	52974505