chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	169200965	169200966	T	G	50	GENIC	homozygous	141420318
2	169201611	169201612	T	A	44	GENIC	homozygous	141420319
2	169203250	169203251	T	G	40	GENIC	homozygous	136365101
2	169203848	169203849	C	T	17	GENIC	homozygous	136365102
2	169203861	169203862	C	T	17	GENIC	heterozygous	403026780
2	169203801	169203802	C		20	GENIC	heterozygous	141333678
2	169203801	169203802	C	T	20	GENIC	homozygous	403026772
2	169203813	169203814	C		18	GENIC	heterozygous	403026773
2	169203813	169203814	C	T	18	GENIC	homozygous	403026774
2	169203848	169203849	C		17	GENIC	heterozygous	403026775
2	169203857	169203858	C	T	17	GENIC	heterozygous	403026776
2	169203857	169203858	C		17	GENIC	homozygous	403026777
2	169203859	169203860	C	T	17	GENIC	heterozygous	403026778
2	169203859	169203860	C		17	GENIC	homozygous	403026779
2	169203861	169203862	C		17	GENIC	homozygous	403026781
2	169204322	169204323	A	G	35	GENIC	homozygous	141420321
2	169204540	169204541	T	G	58	GENIC	possibly homozygous	136365103
2	169204996	169204997	A	G	49	GENIC	homozygous	136365104
2	169205162	169205163	G	A	41	GENIC	homozygous	141420322
2	169206366	169206367	G	C	52	GENIC	homozygous	141420323
2	169203998	169203999	C		36	GENIC	heterozygous	142900369
2	169203831	169203831		CCCTCC	16	GENIC	homozygous	144279973
2	169205718	169205718		T	36	GENIC	possibly homozygous	135959368
2	169203875	169203876	T	C	17	GENIC	homozygous	141136164
2	169203998	169203999	C	A	36	GENIC	homozygous	154006560