chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10495548	10495549	T	C	31	GENIC	homozygous	109634042
19	10495717	10495718	T	C	20	GENIC	homozygous	110169046
19	10495727	10495728	G	T	22	GENIC	possibly homozygous	110058358
19	10495738	10495739	T	C	18	GENIC	homozygous	110169048
19	10495751	10495752	G	A	10	GENIC	homozygous	110169050
19	10495763	10495764	C	A	8	GENIC	homozygous	119596328
19	10496300	10496301	G	T	44	GENIC	homozygous	109634048
19	10496905	10496906	G	C	30	GENIC	homozygous	109634050
19	10498387	10498388	C	T	31	GENIC	homozygous	109634052
19	10499679	10499680	G	A	38	GENIC	homozygous	109634054
19	10500386	10500387	G	T	24	GENIC	homozygous	109634056
19	10505751	10505752	G	A	34	GENIC	possibly homozygous	109634058
19	10498695	10498696	C	G	26	GENIC	possibly homozygous	119722035
19	10505001	10505002	T	C	121	GENIC	heterozygous	110098979
19	10514028	10514029	G	A	8	GENIC	homozygous	109799513
19	10514076	10514077	C	G	5	GENIC	homozygous	109634060
19	10514078	10514079	A	G	5	GENIC	homozygous	109634062
19	10514542	10514543	C	T	41	GENIC	homozygous	109634064
19	10514593	10514594	A	G	39	GENIC	homozygous	109634066
19	10514636	10514637	G	A	45	GENIC	homozygous	109634068