chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	51012677	51012678	T	C	74	GENIC	homozygous	114798391
6	51012701	51012702	C	T	67	GENIC	homozygous	114798392
6	51013095	51013096	G	A	72	GENIC	homozygous	114798393
6	51016654	51016655	A	G	68	GENIC	possibly homozygous	114798394
6	51016821	51016822	C	A	72	GENIC	homozygous	114798395
6	51016825	51016826	T	G	75	GENIC	homozygous	114798396
6	51016852	51016853	A	T	67	GENIC	homozygous	115058974
6	51018256	51018257	C	T	75	GENIC	homozygous	114798397
6	51018631	51018632	G	A	69	GENIC	homozygous	114798398
6	51019303	51019304	C	T	39	GENIC	homozygous	114798399
6	51019621	51019622	G	A	61	GENIC	homozygous	114798400
6	51020253	51020254	G	T	65	GENIC	possibly homozygous	114798401
6	51020288	51020289	C	T	74	GENIC	possibly homozygous	114798402
6	51020954	51020955	G	A	73	GENIC	homozygous	114798403