chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19002600	19002601	A	G	19	GENIC	homozygous	111750550
16	19004584	19004585	A	G	26	GENIC	homozygous	111945808
16	19007092	19007093	T	A	16	GENIC	homozygous	112129042
16	19010938	19010939	G	A	30	GENIC	homozygous	112129044
16	19011816	19011817	A	G	35	GENIC	homozygous	111750560
16	19014343	19014344	T	C	25	GENIC	homozygous	112129046
16	19019688	19019689	G	A	18	GENIC	homozygous	111750564
16	19021195	19021196	T	A	10	GENIC	homozygous	112129048
16	19022977	19022978	C	T	18	GENIC	homozygous	112129050
16	19024906	19024907	G	A	24	GENIC	homozygous	112129052
16	19028855	19028856	C	T	19	GENIC	homozygous	112052620
16	19028857	19028858	T	C	21	GENIC	homozygous	112052621
16	19029015	19029016	G	A	23	GENIC	homozygous	112129054
16	19029383	19029384	A	G	31	GENIC	homozygous	112129056
16	19031072	19031073	G	A	33	GENIC	homozygous	112129058
16	19031726	19031727	T	C	25	GENIC	homozygous	111750572
16	19033931	19033932	G	A	32	GENIC	homozygous	111750574
16	19034877	19034878	T	C	30	GENIC	homozygous	111750576
16	19034971	19034972	A	G	24	GENIC	homozygous	111750578
16	19035710	19035711	A	T	32	GENIC	homozygous	111750580
16	19035965	19035966	T	A	30	GENIC	homozygous	112129060
16	19036878	19036879	T	G	22	GENIC	homozygous	111750582
16	19042307	19042308	A	G	22	GENIC	homozygous	112129062
16	19042692	19042693	C	T	24	GENIC	homozygous	112129065
16	19044211	19044212	T	C	28	GENIC	homozygous	111750586
16	19044347	19044348	C	T	21	GENIC	homozygous	111750588
16	19049503	19049504	C	T	36	GENIC	homozygous	112129067