chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	160232215	160232216	C	T	38	GENIC	homozygous	111791796
3	160232326	160232327	C	G	29	GENIC	homozygous	111791798
3	160232562	160232563	G	A	41	GENIC	homozygous	111791800
3	160232825	160232833	CCAAATGA		37	GENIC	homozygous	127948242
3	160232835	160232835		TTC	37	GENIC	homozygous	127948243
3	160233095	160233096	G	T	40	GENIC	homozygous	111791802
3	160233162	160233163	G	T	50	GENIC	possibly homozygous	111791804
3	160233516	160233518	AA		36	GENIC	homozygous	127948244
3	160233597	160233598	T	C	49	GENIC	homozygous	111791806
3	160233731	160233732	C	T	40	GENIC	homozygous	111791808
3	160233825	160233827	CT		24	GENIC	homozygous	127948245
3	160233878	160233879	G	A	28	GENIC	homozygous	111791810
3	160233997	160233998	T	C	41	GENIC	homozygous	111791812
3	160234061	160234068	CAAAAAA		40	GENIC	homozygous	127948246
3	160234120	160234121	G	A	47	GENIC	homozygous	111791814
3	160234128	160234129	A	G	50	GENIC	homozygous	111791816
3	160234129	160234130	A	T	50	GENIC	homozygous	111791818
3	160234358	160234359	G	A	34	GENIC	homozygous	111791820
3	160234394	160234395	C	T	36	GENIC	homozygous	111791822
3	160234485	160234486	A	G	44	GENIC	homozygous	111791824
3	160234773	160234774	A	G	40	GENIC	homozygous	111791826
3	160234901	160234902	A	T	42	GENIC	homozygous	111791828
3	160235694	160235695	T	C	30	GENIC	homozygous	111791830
3	160236025	160236026	G	A	43	GENIC	homozygous	111791832
3	160237700	160237701	G	A	42	GENIC	homozygous	111791840
3	160237187	160237188	T	A	47	GENIC	homozygous	111791834
3	160237250	160237251	G	A	39	GENIC	homozygous	111791836
3	160237636	160237637	G	A	36	GENIC	homozygous	111791838
3	160237875	160237876	G	A	42	GENIC	homozygous	111791842
3	160237942	160237943	C	T	36	GENIC	homozygous	111791844