chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	174765678	174765679	T	C	35	GENIC	possibly homozygous	120579092
1	174766686	174766687	A	G	19	GENIC	homozygous	120579096
1	174766879	174766880	T	C	21	GENIC	homozygous	120579098
1	174767097	174767098	G	A	25	GENIC	homozygous	120579100
1	174767258	174767259	T	C	25	GENIC	homozygous	120579102
1	174770770	174770771	T	A	27	GENIC	homozygous	120579104
1	174771233	174771234	C	A	34	GENIC	homozygous	120579106
1	174772157	174772158	A	G	20	GENIC	possibly homozygous	120579108
1	174772470	174772471	G	A	30	GENIC	possibly homozygous	120579110
1	174776250	174776251	T	C	24	GENIC	homozygous	120579234
1	174777911	174777912	A	T	16	GENIC	homozygous	120579236
1	174777928	174777929	A	T	21	GENIC	homozygous	120579238
1	174778342	174778343	A	C	26	GENIC	possibly homozygous	120579240
1	174779127	174779128	C	A	33	GENIC	homozygous	120579242
1	174779496	174779497	C	A	25	GENIC	possibly homozygous	120579244
1	174779527	174779528	A	G	18	GENIC	possibly homozygous	120579246
1	174780244	174780245	A	G	38	GENIC	homozygous	108393031
1	174781363	174781364	G	A	26	GENIC	possibly homozygous	108393037
1	174781736	174781737	T	C	26	GENIC	homozygous	108393039
1	174783246	174783247	G	A	34	GENIC	homozygous	120579252
1	174783693	174783694	C	T	29	GENIC	possibly homozygous	120579254
1	174784341	174784342	A	G	26	GENIC	possibly homozygous	120579256
1	174784922	174784923	A	T	24	GENIC	homozygous	120579258
1	174787642	174787643	G	T	26	GENIC	homozygous	120579260
1	174788601	174788602	A	G	20	GENIC	possibly homozygous	108393045
1	174782144	174782145	C	A	33	GENIC	possibly homozygous	120901058