chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	166006936	166006937	G	A	68	GENIC	heterozygous	114162752
5	166006961	166006962	T	C	74	GENIC	heterozygous	114081883
5	166006963	166006964	C	A	74	GENIC	heterozygous	114081884
5	166006969	166006970	T	C	83	GENIC	heterozygous	114081885
5	166006972	166006973	T	C	85	GENIC	heterozygous	114081886
5	166006981	166006982	T	C	92	GENIC	heterozygous	114081887
5	166007009	166007010	C	T	104	GENIC	heterozygous	114081888
5	166007016	166007017	T	A	109	GENIC	heterozygous	114081889
5	166007028	166007029	A	C	108	GENIC	heterozygous	114081890
5	166007046	166007047	G	C	108	GENIC	heterozygous	114162753
5	166007070	166007071	T	C	88	GENIC	heterozygous	114162754
5	166007080	166007081	T	G	76	GENIC	heterozygous	114081891
5	166007083	166007084	C	A	73	GENIC	heterozygous	114081892
5	166007090	166007091	A	C	74	GENIC	heterozygous	114081893
5	166007093	166007094	C	G	73	GENIC	heterozygous	114081894
5	166007099	166007100	A	C	72	GENIC	heterozygous	114081895
5	166087492	166087493	C	A	22	GENIC	possibly homozygous	114162755
5	166087495	166087496	C	A	23	GENIC	heterozygous	114162756
5	166111749	166111750	T	C	30	GENIC	possibly homozygous	114081897
5	166132829	166132830	A	C	38	GENIC	possibly homozygous	114081898