chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	52366377	52366378	A	C	31	GENIC	homozygous	109728839
19	52372898	52372899	G	T	10	GENIC	homozygous	109788734
19	52372897	52372898	T	G	9	GENIC	homozygous	109788732
19	52374209	52374210	G	C	13	GENIC	homozygous	109728841
19	52374548	52374549	A	C	28	GENIC	homozygous	109728843
19	52374598	52374599	A	C	27	GENIC	homozygous	109824879
19	52378668	52378669	A	T	19	GENIC	homozygous	109728845
19	52378669	52378670	A	C	20	GENIC	homozygous	109728847
19	52378670	52378671	A	C	20	GENIC	homozygous	109728849
19	52378695	52378696	T	C	22	GENIC	homozygous	109728851
19	52378710	52378711	G	C	22	GENIC	homozygous	109728853
19	52404198	52404199	G	C	19	GENIC	homozygous	109874813
19	52374198	52374199	A	C	9	GENIC	homozygous	109963009
19	52374206	52374207	C	A	11	GENIC	homozygous	109963011