chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44168002	44168003	C	T	12	GENIC	homozygous	109818614
19	44168436	44168437	G	T	13	GENIC	homozygous	109818616
19	44168474	44168475	A	T	11	GENIC	homozygous	109709768
19	44169835	44169836	T	C	14	GENIC	homozygous	109709774
19	44169874	44169875	A	G	14	GENIC	homozygous	109818618
19	44172288	44172289	C	T	19	GENIC	homozygous	109709780
19	44172630	44172631	C	T	12	GENIC	homozygous	109709782
19	44172770	44172771	C	T	9	GENIC	homozygous	109818620
19	44172924	44172925	G	C	11	GENIC	homozygous	109818622
19	44173685	44173686	C	T	13	GENIC	homozygous	109709784
19	44173706	44173707	T	C	16	GENIC	homozygous	109709786
19	44173850	44173851	T	A	11	GENIC	homozygous	109818624
19	44173975	44173976	A	G	7	GENIC	homozygous	109709790
19	44174154	44174155	C	A	14	GENIC	homozygous	109709792
19	44174252	44174253	C	T	11	GENIC	homozygous	109709794