chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	163794373	163794374	A	G	81	GENIC	homozygous	108348942
1	163794494	163794495	C	T	71	GENIC	homozygous	108952570
1	163794901	163794901		GATTT	72	GENIC	homozygous	127452041
1	163796037	163796038	C		59	GENIC	homozygous	131578286
1	163796316	163796317	T	C	38	GENIC	homozygous	108952571
1	163796414	163796415	C	T	41	GENIC	possibly homozygous	108952573
1	163801497	163801498	T	C	69	GENIC	homozygous	120508819
1	163801528	163801529	A	G	69	GENIC	homozygous	120508820
1	163802726	163802727	T	C	58	GENIC	homozygous	108952574
1	163803258	163803259	C	T	61	GENIC	homozygous	108348948
1	163803657	163803658	G	A	46	GENIC	homozygous	120508821
1	163803811	163803812	A	G	39	GENIC	homozygous	130847369
1	163803887	163803888	C	T	62	GENIC	homozygous	125370931
1	163804301	163804302	C	A	65	GENIC	homozygous	120487136
1	163804382	163804383	C	T	67	GENIC	homozygous	120487137
1	163805423	163805424	C	A	49	GENIC	homozygous	120487138
1	163805913	163805914	G	A	53	GENIC	homozygous	108348954
1	163808445	163808446	T	C	60	GENIC	homozygous	108348960
1	163808924	163808925	G	A	49	GENIC	homozygous	120487139
1	163808925	163808926	A	C	50	GENIC	homozygous	108348961
1	163809349	163809350	C	A	45	GENIC	homozygous	108348963
1	163809769	163809770	A	G	63	GENIC	homozygous	108348965
1	163809779	163809780	C	T	63	GENIC	homozygous	108348967
1	163810641	163810642	G	T	52	GENIC	homozygous	120487140
1	163810650	163810651	A	G	58	GENIC	homozygous	120487141
1	163813384	163813385	T	C	45	GENIC	homozygous	108348977
1	163796381	163796381		GT	25	GENIC	possibly homozygous	131989812
1	163803073	163803074	G		60	GENIC	homozygous	130826183
1	163805136	163805137	C		69	GENIC	homozygous	130826184
1	163810224	163810224		AGGT	50	GENIC	possibly homozygous	130826185