chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	163941762	163941763	A	AT	15	GENIC	homozygous	59193597
2	163943019	163943020	G	A	42	GENIC	homozygous	59193598
2	163944190	163944191	A	G	21	GENIC	homozygous	59193599
2	163944194	163944195	G	C	22	GENIC	homozygous	59193600
2	163944271	163944272	C	T	35	GENIC	homozygous	59193601
2	163944881	163944882	T	TGG	6	GENIC	homozygous	59193603
2	163946584	163946585	G	A	29	GENIC	homozygous	59193605
2	163948584	163948585	A	G	31	GENIC	homozygous	59193608
2	163950022	163950023	C	T	37	GENIC	homozygous	59193609
2	163950110	163950111	A	C	43	GENIC	homozygous	59193610
2	163951120	163951121	A	G	29	GENIC	homozygous	59193613
2	163952544	163952545	A	-	32	GENIC	homozygous	59193618
2	163952640	163952641	G	A	36	GENIC	homozygous	59193619
2	163952653	163952654	G	C	36	GENIC	homozygous	59193620
2	163952658	163952659	T	C	36	GENIC	homozygous	59193621
2	163952688	163952689	G	A	35	GENIC	homozygous	59193622
2	163953529	163953530	G	C	24	GENIC	homozygous	59193623
2	163953531	163953532	G	C	24	GENIC	homozygous	59193624
2	163953533	163953534	G	C	24	GENIC	homozygous	59193625
2	163953911	163953912	C	T	47	GENIC	homozygous	59193626
2	163955156	163955172	GCCACACAGTGGGTCT	----------------	3	GENIC	homozygous	60893019
2	163957919	163957920	C	T	13	GENIC	homozygous	59193627
2	163958221	163958222	T	-	23	GENIC	homozygous	59193628
2	163958321	163958322	C	T	17	GENIC	homozygous	59193629
2	163958511	163958512	G	C	26	GENIC	homozygous	59193630
2	163958544	163958545	G	C	25	GENIC	homozygous	59193631
2	163960519	163960520	T	C	20	GENIC	homozygous	59193632
2	163961703	163961704	T	C	31	GENIC	homozygous	59193633
2	163950877	163950879	AC	--	22	GENIC	possibly homozygous	60504792
2	163951608	163951610	CA	--	9	GENIC	homozygous	60504793