chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10342925	10342926	G	A	20	GENIC	homozygous	46058614
19	10343261	10343262	C	CA	6	GENIC	homozygous	46058615
19	10343621	10343622	T	TATCCATCC	13	GENIC	homozygous	46058616
19	10343725	10343726	G	T	27	GENIC	homozygous	46058624
19	10343888	10343889	A	G	1	GENIC	homozygous	46208006
19	10346304	10346305	T	C	20	GENIC	possibly homozygous	46058626
19	10346695	10346696	G	A	16	GENIC	possibly homozygous	46058627
19	10346731	10346732	T	TTG	4	GENIC	heterozygous	46058628
19	10348092	10348093	C	T	23	GENIC	homozygous	46058630
19	10349274	10349275	T	C	24	GENIC	homozygous	46058631
19	10350534	10350535	A	G	21	GENIC	homozygous	46058632
19	10353140	10353141	G	T	21	GENIC	possibly homozygous	46058633
19	10355625	10355626	C	CCCAGTTATTT	4	GENIC	homozygous	46058635
19	10357598	10357599	T	C	22	GENIC	possibly homozygous	46058636