chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	146715354	146715355	T	G	27	GENIC	homozygous	108277940
1	146715881	146715882	T	C	15	GENIC	homozygous	108277942
1	146717417	146717418	T	G	33	GENIC	homozygous	108277944
1	146719020	146719021	A	G	28	GENIC	homozygous	108277946
1	146721936	146721937	C	A	42	GENIC	homozygous	108277948
1	146725911	146725912	A	G	20	GENIC	homozygous	108277952
1	146726394	146726395	A	G	23	GENIC	homozygous	108277954
1	146726437	146726438	T	C	23	GENIC	homozygous	108277956
1	146726541	146726542	T	G	25	GENIC	homozygous	108277958
1	146727375	146727376	G	A	35	GENIC	homozygous	108277960
1	146727468	146727469	T	C	24	GENIC	homozygous	108277962
1	146727490	146727491	C	T	22	GENIC	homozygous	108277964
1	146727536	146727537	A	G	30	GENIC	homozygous	108277966
1	146727748	146727749	T	G	23	GENIC	homozygous	109145166
1	146728779	146728780	A	C	15	GENIC	possibly homozygous	108277974
1	146729085	146729086	A	G	13	GENIC	homozygous	108277976
1	146729199	146729200	C	G	11	GENIC	homozygous	108277978
1	146729612	146729613	G	A	34	GENIC	homozygous	108277980
1	146731332	146731333	G	A	24	GENIC	homozygous	108277982
1	146731392	146731393	T	C	29	GENIC	homozygous	108277984
1	146731420	146731421	T	C	33	GENIC	homozygous	108277986
1	146731647	146731648	T	C	27	GENIC	homozygous	108277988
1	146731963	146731964	G	A	25	GENIC	homozygous	108277990
1	146732569	146732570	T	C	39	GENIC	homozygous	108277992
1	146733131	146733132	G	A	12	GENIC	homozygous	108277994
1	146733975	146733976	C	T	14	GENIC	homozygous	108277996
1	146734078	146734079	A	G	21	GENIC	homozygous	108277998
1	146734631	146734632	T	C	28	GENIC	homozygous	108278000
1	146735783	146735784	G	A	30	GENIC	homozygous	108278002