chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	33176474	33176475	C	T	38	GENIC	homozygous	140446800
19	33177208	33177208		CTAT	36	GENIC	homozygous	140387018
19	33177899	33177902	AGC		39	GENIC	homozygous	140387019
19	33178154	33178155	G	A	38	GENIC	homozygous	140446801
19	33178975	33178975		TTTTG	36	GENIC	homozygous	140387020
19	33179546	33179547	A	G	55	GENIC	homozygous	140446802
19	33180021	33180022	A	G	44	GENIC	homozygous	140446803
19	33180243	33180244	A	G	51	GENIC	homozygous	140446804
19	33180636	33180637	C	T	48	GENIC	homozygous	140446805
19	33181223	33181224	T	C	52	GENIC	homozygous	140446806