chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	109817959	109817960	G	T	19	GENIC	homozygous	114443622
13	109818058	109818059	G	A	21	GENIC	homozygous	114443624
13	109818589	109818590	T	C	24	GENIC	homozygous	114443626
13	109820299	109820300	A	G	28	GENIC	homozygous	114991541
13	109820447	109820448	T	C	10	GENIC	homozygous	118468658
13	109820450	109820451	T	A	10	GENIC	homozygous	118468659
13	109820576	109820577	T	C	13	GENIC	homozygous	114443628
13	109820828	109820829	C	G	18	GENIC	homozygous	114443630
13	109820841	109820842	T	A	16	GENIC	homozygous	114443632
13	109820934	109820935	G	A	13	GENIC	homozygous	114443634
13	109820975	109820976	T	A	14	GENIC	homozygous	114443636
13	109847896	109847897	A	G	6	GENIC	homozygous	118468661
13	109848752	109848753	G	A	2	GENIC	homozygous	130115508
13	109848503	109848504	G	A	2	GENIC	homozygous	129114881
13	109820470	109820471	C	T	11	GENIC	homozygous	115035691
13	109846453	109846459	GGGGGT		5	GENIC	homozygous	129096932
13	109820498	109820498		C	12	GENIC	homozygous	129096929
13	109821329	109821332	TTA		18	GENIC	homozygous	129096930
13	109846411	109846417	GGTGGT		4	GENIC	homozygous	129096931
13	109841789	109841790	G	C	5	GENIC	homozygous	129114879
13	109847526	109847527	C	T	4	GENIC	homozygous	129114880