chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19382908	19382909	A	T	26	GENIC	homozygous	50098909
12	19383277	19383281	TTTT	----	10	GENIC	homozygous	50284575
12	19383292	19383293	T	G	15	GENIC	homozygous	50536724
12	19383394	19383395	A	G	8	GENIC	homozygous	50098915
12	19383632	19383633	T	C	13	GENIC	homozygous	50098917
12	19384278	19384279	A	AT	11	GENIC	homozygous	50483202
12	19384710	19384711	A	ATGTG	3	GENIC	homozygous	50536726
12	19384747	19384748	G	T	8	GENIC	homozygous	50483206
12	19387032	19387033	T	C	19	GENIC	homozygous	50098935
12	19387195	19387196	G	GGTGT	9	GENIC	heterozygous	50536728
12	19387195	19387196	G	GGTGTGT	9	GENIC	heterozygous	50536730
12	19387195	19387196	G	GGTGTGTGT	9	GENIC	heterozygous	50536732
12	19387896	19387897	G	GCATCTC	20	GENIC	homozygous	50098939
12	19388323	19388324	G	T	27	GENIC	homozygous	50368775
12	19388722	19388723	G	A	31	GENIC	homozygous	50483208
12	19389102	19389103	T	C	28	GENIC	homozygous	50098941
12	19389126	19389127	T	C	31	GENIC	homozygous	50098943
12	19390611	19390612	A	G	27	GENIC	homozygous	50098945
12	19390920	19390921	C	A	28	GENIC	homozygous	50483210
12	19390999	19391000	T	C	24	GENIC	homozygous	50098947