chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10948953	10948954	T	C	49	GENIC	homozygous	140404568
19	10953188	10953189	C	T	45	GENIC	homozygous	140404569
19	10954531	10954532	C	A	53	GENIC	homozygous	140404570
19	10954932	10954933	G	C	56	GENIC	homozygous	140404571
19	10955090	10955091	G	A	49	GENIC	homozygous	140404572
19	10960186	10960188	AA		9	GENIC	heterozygous	145932326
19	10966040	10966041	A	C	49	GENIC	homozygous	140404573
19	10968222	10968223	C	T	36	GENIC	homozygous	140404574
19	10968567	10968568	C	T	44	GENIC	homozygous	140404575
19	10969041	10969042	C	T	44	GENIC	homozygous	140404576
19	10970073	10970073		CTC	49	GENIC	possibly homozygous	140376582
19	10970762	10970763	C	T	41	GENIC	homozygous	140404577
19	10970913	10970914	C	T	39	GENIC	homozygous	140404578
19	10971496	10971497	T	A	33	GENIC	homozygous	140404579
19	10972495	10972496	G	A	47	GENIC	homozygous	140404580