chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	44167432	44167433	A	G	23	GENIC	homozygous	109784619
19	44167916	44167917	T	A	33	GENIC	homozygous	109784621
19	44167986	44167987	T	A	16	GENIC	homozygous	109870490
19	44167996	44167997	G	T	2	GENIC	homozygous	109870492
19	44168474	44168475	A	T	24	GENIC	homozygous	109709768
19	44168640	44168641	G	C	23	GENIC	homozygous	109784623
19	44169690	44169691	G	A	33	GENIC	homozygous	109709772
19	44169835	44169836	T	C	28	GENIC	homozygous	109709774
19	44172288	44172289	C	T	26	GENIC	homozygous	109709780
19	44172630	44172631	C	T	27	GENIC	homozygous	109709782
19	44173685	44173686	C	T	42	GENIC	homozygous	109709784
19	44173706	44173707	T	C	35	GENIC	homozygous	109709786
19	44173975	44173976	A	G	14	GENIC	homozygous	109709790
19	44174154	44174155	C	A	20	GENIC	homozygous	109709792
19	44174252	44174253	C	T	27	GENIC	homozygous	109709794
19	44174378	44174379	C	T	29	GENIC	homozygous	109784625
19	44175406	44175407	G	A	14	GENIC	homozygous	109784627
19	44175411	44175412	T	C	13	GENIC	homozygous	109709796