chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10495548	10495549	T	C	30	GENIC	homozygous	109634042
19	10496300	10496301	G	T	42	GENIC	homozygous	109634048
19	10496905	10496906	G	C	27	GENIC	homozygous	109634050
19	10498387	10498388	C	T	28	GENIC	homozygous	109634052
19	10499679	10499680	G	A	38	GENIC	homozygous	109634054
19	10500386	10500387	G	T	22	GENIC	homozygous	109634056
19	10514076	10514077	C	G	5	GENIC	homozygous	109634060
19	10514078	10514079	A	G	5	GENIC	homozygous	109634062
19	10514542	10514543	C	T	40	GENIC	homozygous	109634064
19	10514593	10514594	A	G	39	GENIC	homozygous	109634066
19	10514636	10514637	G	A	44	GENIC	homozygous	109634068
19	10514028	10514029	G	A	8	GENIC	homozygous	109799513