chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20020634	20020635	T	C	16	GENIC	homozygous	111751785
16	20021259	20021260	C	A	16	GENIC	homozygous	111948032
16	20021432	20021433	G	A	19	GENIC	homozygous	111948034
16	20021643	20021644	T	C	32	GENIC	homozygous	111948036
16	20021779	20021780	G	A	21	GENIC	homozygous	111948038
16	20022511	20022512	C	T	24	GENIC	homozygous	112052726
16	20022752	20022753	G	C	14	GENIC	homozygous	111948040
16	20022891	20022892	T	C	27	GENIC	homozygous	111948042
16	20023254	20023255	C	T	30	GENIC	possibly homozygous	111948044
16	20023286	20023287	T	C	32	GENIC	homozygous	111751789
16	20023351	20023352	A	G	23	GENIC	homozygous	111751791
16	20023422	20023423	T	C	26	GENIC	homozygous	111948046
16	20023755	20023756	T	C	45	GENIC	homozygous	111948048
16	20023862	20023863	G	A	36	GENIC	homozygous	111948050
16	20023921	20023922	T	G	35	GENIC	homozygous	111948052
16	20023932	20023933	A	C	37	GENIC	homozygous	111948054
16	20023941	20023942	C	G	39	GENIC	homozygous	111948056
16	20024525	20024526	C	T	21	GENIC	homozygous	111948058
16	20024751	20024752	T	C	38	GENIC	possibly homozygous	111948060
16	20025072	20025073	A	G	30	GENIC	homozygous	111948062