chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19382908	19382909	A	T	26	GENIC	homozygous	50098909
12	19383297	19383298	T	TTG	6	GENIC	heterozygous	50098911
12	19383301	19383303	TG	--	15	GENIC	heterozygous	50098913
12	19383394	19383395	A	G	37	GENIC	homozygous	50098915
12	19383404	19383405	G	GT	24	GENIC	homozygous	50368765
12	19383481	19383492	TTAGGGCTCTC	-----------	6	GENIC	homozygous	50368767
12	19383605	19383606	A	AT	19	GENIC	heterozygous	50284578
12	19383605	19383606	A	ATT	19	GENIC	heterozygous	50284579
12	19383632	19383633	T	C	41	GENIC	possibly homozygous	50098917
12	19384279	19384280	T	-	24	GENIC	heterozygous	50098919
12	19384634	19384638	CTGG	----	9	GENIC	heterozygous	50098921
12	19384654	19384656	GT	--	8	GENIC	homozygous	50368769
12	19384746	19384747	G	-	18	GENIC	homozygous	50368771
12	19386803	19386804	A	G	49	GENIC	homozygous	50368773
12	19387032	19387033	T	C	30	GENIC	homozygous	50098935
12	19387228	19387230	AC	--	15	GENIC	heterozygous	50098937
12	19387896	19387897	G	GCATCTC	7	GENIC	homozygous	50098939
12	19388323	19388324	G	T	38	GENIC	homozygous	50368775
12	19389102	19389103	T	C	30	GENIC	homozygous	50098941
12	19389126	19389127	T	C	32	GENIC	homozygous	50098943
12	19389842	19389843	A	G	36	GENIC	homozygous	50368777
12	19390445	19390446	G	C	37	GENIC	homozygous	50368779
12	19390611	19390612	A	G	32	GENIC	homozygous	50098945
12	19390999	19391000	T	C	25	GENIC	homozygous	50098947