chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10342925	10342926	G	A	34	GENIC	homozygous	46058614
19	10343261	10343262	C	CA	28	GENIC	homozygous	46058615
19	10343621	10343622	T	TATCCATCC	27	GENIC	homozygous	46058616
19	10343725	10343726	G	T	49	GENIC	homozygous	46058624
19	10343877	10343883	CACACC	------	14	GENIC	heterozygous	46397183
19	10343886	10343887	C	G	17	GENIC	possibly homozygous	46397185
19	10343888	10343889	A	G	34	GENIC	possibly homozygous	46208006
19	10346304	10346305	T	C	47	GENIC	homozygous	46058626
19	10346695	10346696	G	A	18	GENIC	homozygous	46058627
19	10346731	10346732	T	TTG	10	GENIC	homozygous	46058628
19	10346799	10346800	C	-	1	GENIC	homozygous	46485776
19	10346822	10346830	TTTGGTTC	--------	3	GENIC	heterozygous	46485779
19	10348092	10348093	C	T	26	GENIC	homozygous	46058630
19	10349274	10349275	T	C	35	GENIC	homozygous	46058631
19	10350534	10350535	A	G	19	GENIC	homozygous	46058632
19	10353140	10353141	G	T	26	GENIC	homozygous	46058633
19	10355224	10355225	T	TTGTG	12	GENIC	heterozygous	46058634
19	10355224	10355225	T	TTG	12	GENIC	heterozygous	46507199
19	10355625	10355626	C	CCCAGTTATTT	23	GENIC	homozygous	46058635
19	10355671	10355672	A	ACTCTCTCT	12	GENIC	heterozygous	46397187
19	10355671	10355672	A	ACTCTCTCTCT	12	GENIC	heterozygous	46397189
19	10356209	10356210	T	A	37	GENIC	possibly homozygous	46365578
19	10357598	10357599	T	C	27	GENIC	homozygous	46058636