chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	34772152	34772153	C	T	21	GENIC	homozygous	145078628
19	34777332	34777333	T	A	21	GENIC	homozygous	145078629
19	34777700	34777701	A	C	10	GENIC	homozygous	145078630
19	34777906	34777907	C	A	3	GENIC	homozygous	145078631
19	34778130	34778131	T	C	18	GENIC	homozygous	145078632
19	34778310	34778311	A	C	21	GENIC	homozygous	145078633
19	34778350	34778351	C	T	15	GENIC	homozygous	145078634
19	34778353	34778354	T	C	16	GENIC	homozygous	145078635
19	34778433	34778434	A	G	19	GENIC	homozygous	145078636
19	34778537	34778538	A	G	17	GENIC	homozygous	145078637
19	34778618	34778619	T	G	20	GENIC	homozygous	145078638
19	34778765	34778766	A	G	18	GENIC	homozygous	145078639
19	34778839	34778840	A	C	20	GENIC	homozygous	145078640
19	34778877	34778878	A	G	14	GENIC	homozygous	145078641
19	34778904	34778905	C	T	12	GENIC	homozygous	145078642
19	34781574	34781575	C		13	GENIC	homozygous	144207687
19	34781894	34781895	G	A	16	GENIC	homozygous	145078643
19	34777837	34777848	TTTTTTTTTGT		13	GENIC	homozygous	145068636
19	34778924	34778927	CTC		12	GENIC	homozygous	145068637
19	34777914	34777915	A	T	3	GENIC	homozygous	148417447