chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19382446	19382447	G	A	48	GENIC	homozygous	50284573
12	19382530	19382531	G	A	38	GENIC	homozygous	50284574
12	19382908	19382909	A	T	73	GENIC	homozygous	50098909
12	19383277	19383281	TTTT	----	13	GENIC	heterozygous	50284575
12	19383297	19383298	T	TTG	10	GENIC	heterozygous	50098911
12	19383297	19383298	T	TG	10	GENIC	heterozygous	50284576
12	19383301	19383303	TG	--	22	GENIC	heterozygous	50098913
12	19383394	19383395	A	G	35	GENIC	homozygous	50098915
12	19383591	19383592	G	T	47	GENIC	homozygous	50284577
12	19383605	19383606	A	AT	28	GENIC	heterozygous	50284578
12	19383605	19383606	A	ATT	28	GENIC	heterozygous	50284579
12	19383632	19383633	T	C	52	GENIC	possibly homozygous	50098917
12	19384634	19384638	CTGG	----	10	GENIC	heterozygous	50098921
12	19384650	19384651	C	G	9	GENIC	heterozygous	50098925
12	19384653	19384654	G	T	9	GENIC	heterozygous	50098927
12	19384653	19384654	G	GGTGTGT	3	GENIC	homozygous	50098929
12	19384675	19384679	CTCA	----	7	GENIC	heterozygous	50098931
12	19387032	19387033	T	C	47	GENIC	homozygous	50098935
12	19387196	19387198	GT	--	17	GENIC	homozygous	50284580
12	19387228	19387230	AC	--	21	GENIC	heterozygous	50098937
12	19387529	19387530	C	T	63	GENIC	possibly homozygous	50284581
12	19387896	19387897	G	GCATCTC	15	GENIC	homozygous	50098939
12	19388529	19388530	G	A	52	GENIC	homozygous	50284582
12	19388958	19388959	T	C	63	GENIC	possibly homozygous	50284583
12	19389102	19389103	T	C	44	GENIC	homozygous	50098941
12	19389126	19389127	T	C	42	GENIC	homozygous	50098943
12	19389846	19389847	G	A	51	GENIC	homozygous	50284584
12	19390124	19390125	C	T	58	GENIC	homozygous	50284585
12	19390611	19390612	A	G	60	GENIC	homozygous	50098945
12	19390731	19390739	AGCGGGGC	--------	19	GENIC	homozygous	50284586
12	19390967	19390968	G	A	50	GENIC	homozygous	50284587
12	19390999	19391000	T	C	48	GENIC	homozygous	50098947