chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	239269637	239269638	A		43	GENIC	possibly homozygous	127495564
1	239270359	239270360	G	C	40	GENIC	homozygous	109453163
1	239274046	239274047	A		29	GENIC	heterozygous	127495566
1	239277036	239277036		GCG	28	GENIC	homozygous	134505300
1	239277496	239277499	TTA		30	GENIC	homozygous	134172790
1	239277788	239277789	T	C	10	GENIC	homozygous	108585842
1	239278068	239278069	C		39	GENIC	homozygous	127495568
1	239279063	239279064	C	A	42	GENIC	homozygous	108585845
1	239279501	239279502	A	G	53	GENIC	homozygous	109453165
1	239281586	239281587	T	C	56	GENIC	homozygous	108585846
1	239291808	239291809	T	A	43	GENIC	homozygous	108585859
1	239294574	239294575	G	A	49	GENIC	homozygous	108585863
1	239298218	239298219	T	C	56	GENIC	homozygous	108585864
1	239299083	239299084	A	G	45	GENIC	homozygous	108585866
1	239299194	239299195	T	C	47	GENIC	homozygous	108585867
1	239299705	239299706	G	A	46	GENIC	homozygous	109453166
1	239288389	239288389		GC	45	GENIC	homozygous	127495571
1	239296354	239296357	TTA		35	GENIC	possibly homozygous	134172791