chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37090386	37090387	T	G	49	GENIC	homozygous	109692980
19	37090677	37090678	C	T	33	GENIC	homozygous	109692982
19	37091567	37091568	A	T	41	GENIC	homozygous	109924568
19	37094374	37094375	T	C	49	GENIC	homozygous	119629134
19	37097054	37097055	C	T	41	GENIC	homozygous	109692984
19	37097672	37097673	T	G	25	GENIC	homozygous	109692986
19	37097693	37097694	C	T	33	GENIC	homozygous	109692988
19	37098535	37098536	C	G	30	GENIC	possibly homozygous	109692990
19	37100541	37100542	C	T	43	GENIC	homozygous	109692992
19	37101925	37101926	T	A	29	GENIC	possibly homozygous	109924570
19	37102696	37102697	G	A	46	GENIC	possibly homozygous	109692994
19	37106084	37106085	G	A	33	GENIC	possibly homozygous	109692996
19	37106118	37106119	A	C	41	GENIC	heterozygous	119629135
19	37107226	37107227	A	G	39	GENIC	homozygous	109692998
19	37107751	37107752	T	A	43	GENIC	homozygous	109693000
19	37107777	37107778	C	T	44	GENIC	homozygous	109693002
19	37111167	37111168	A	C	65	GENIC	homozygous	109693004
19	37111432	37111433	C	T	46	GENIC	possibly homozygous	110049475