chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	163794373	163794374	A	G	16	GENIC	homozygous	108348942
1	163794494	163794495	C	T	16	GENIC	possibly homozygous	108952570
1	163796316	163796317	T	C	22	GENIC	homozygous	108952571
1	163798553	163798554	G	C	25	GENIC	homozygous	109339439
1	163802720	163802721	G	A	19	GENIC	homozygous	109339441
1	163802726	163802727	T	C	19	GENIC	homozygous	108952574
1	163802821	163802822	G	A	24	GENIC	homozygous	109339443
1	163803258	163803259	C	T	22	GENIC	homozygous	108348948
1	163803411	163803412	G	A	31	GENIC	homozygous	108348950
1	163804708	163804709	T	C	35	GENIC	possibly homozygous	109339445
1	163805187	163805188	G	T	33	GENIC	homozygous	109339447
1	163805913	163805914	G	A	29	GENIC	homozygous	108348954
1	163806140	163806141	C	T	34	GENIC	homozygous	109339449
1	163806510	163806511	C	T	35	GENIC	possibly homozygous	109339451
1	163808445	163808446	T	C	27	GENIC	homozygous	108348960
1	163808772	163808773	G	T	24	GENIC	homozygous	109339453
1	163808925	163808926	A	C	26	GENIC	homozygous	108348961
1	163809349	163809350	C	A	37	GENIC	homozygous	108348963
1	163809769	163809770	A	G	20	GENIC	homozygous	108348965
1	163810393	163810394	C	T	23	GENIC	homozygous	108348969
1	163810715	163810716	G	A	27	GENIC	possibly homozygous	109339455
1	163811372	163811373	A	G	26	GENIC	possibly homozygous	108348971
1	163811791	163811792	G	A	40	GENIC	possibly homozygous	108348973
1	163812163	163812164	C	T	22	GENIC	homozygous	108348975
1	163813384	163813385	T	C	10	GENIC	homozygous	108348977