chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	156591976	156591977	A	C	56	GENIC	homozygous	135716767
1	156592584	156592585	C	T	58	GENIC	homozygous	135716768
1	156593214	156593215	C	T	67	GENIC	homozygous	135716769
1	156593251	156593252	G	T	65	GENIC	homozygous	135716770
1	156593382	156593383	T		51	GENIC	homozygous	135439039
1	156595242	156595243	A	C	55	GENIC	homozygous	135716771
1	156595939	156595940	A	T	38	GENIC	homozygous	135716772
1	156597381	156597382	A	G	70	GENIC	homozygous	135716773
1	156597689	156597690	G	A	71	GENIC	homozygous	135716774
1	156599305	156599306	A	C	57	GENIC	homozygous	135716775
1	156601206	156601207	T		45	GENIC	homozygous	135439040
1	156601592	156601593	T	C	70	GENIC	homozygous	135716776
1	156608492	156608493	T	C	39	GENIC	homozygous	135716777
1	156608596	156608597	C	T	52	GENIC	homozygous	135716778
1	156608842	156608842		T	47	GENIC	homozygous	135439041
1	156609917	156609918	C		67	GENIC	homozygous	135439042
1	156612454	156612455	T	C	44	GENIC	homozygous	135716779
1	156613774	156613775	C	A	71	GENIC	homozygous	135716780
1	156613944	156613945	A	G	64	GENIC	homozygous	135716781
1	156615779	156615780	C	T	51	GENIC	homozygous	135716782
1	156613169	156613170	G		31	GENIC	possibly homozygous	402969324
1	156612699	156612700	A	G	12	GENIC	homozygous	153879801
1	156613169	156613170	G	A	31	GENIC	heterozygous	153879802
1	156612699	156612700	A		12	GENIC	heterozygous	402969323