chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10495548	10495549	T	C	29	GENIC	homozygous	109634042
19	10496300	10496301	G	T	31	GENIC	homozygous	109634048
19	10496905	10496906	G	C	13	GENIC	homozygous	109634050
19	10498387	10498388	C	T	21	GENIC	homozygous	109634052
19	10499679	10499680	G	A	17	GENIC	homozygous	109634054
19	10500386	10500387	G	T	20	GENIC	homozygous	109634056
19	10505751	10505752	G	A	33	GENIC	homozygous	109634058
19	10514076	10514077	C	G	2	GENIC	homozygous	109634060
19	10514078	10514079	A	G	2	GENIC	homozygous	109634062
19	10514542	10514543	C	T	18	GENIC	homozygous	109634064
19	10514593	10514594	A	G	18	GENIC	homozygous	109634066
19	10514636	10514637	G	A	24	GENIC	homozygous	109634068
19	10514028	10514029	G	A	2	GENIC	homozygous	109799513
19	10514019	10514020	G	A	2	GENIC	homozygous	110107321