chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19382908	19382909	A	T	22	GENIC	homozygous	50098909
12	19383144	19383148	GTGT	----	2	GENIC	homozygous	50438209
12	19383277	19383281	TTTT	----	5	GENIC	homozygous	50284575
12	19383297	19383298	T	TG	5	GENIC	homozygous	50284576
12	19383301	19383303	TG	--	12	GENIC	heterozygous	50098913
12	19383394	19383395	A	G	21	GENIC	homozygous	50098915
12	19383605	19383606	A	AT	15	GENIC	heterozygous	50284578
12	19383632	19383633	T	C	14	GENIC	possibly homozygous	50098917
12	19384278	19384279	A	AT	25	GENIC	possibly homozygous	50483202
12	19384634	19384638	CTGG	----	14	GENIC	heterozygous	50098921
12	19384644	19384645	A	G	9	GENIC	heterozygous	50098923
12	19384653	19384654	G	GGTGTGT	6	GENIC	homozygous	50098929
12	19384675	19384679	CTCA	----	12	GENIC	heterozygous	50098931
12	19384724	19384725	A	G	12	GENIC	homozygous	50483204
12	19384747	19384748	G	T	12	GENIC	homozygous	50483206
12	19387032	19387033	T	C	42	GENIC	homozygous	50098935
12	19387228	19387230	AC	--	30	GENIC	heterozygous	50098937
12	19387896	19387897	G	GCATCTC	10	GENIC	homozygous	50098939
12	19388323	19388324	G	T	43	GENIC	homozygous	50368775
12	19388722	19388723	G	A	43	GENIC	homozygous	50483208
12	19389102	19389103	T	C	30	GENIC	homozygous	50098941
12	19389126	19389127	T	C	34	GENIC	homozygous	50098943
12	19390611	19390612	A	G	32	GENIC	homozygous	50098945
12	19390920	19390921	C	A	31	GENIC	homozygous	50483210
12	19390999	19391000	T	C	37	GENIC	homozygous	50098947