chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	245478671	245478672	C	T	27	GENIC	homozygous	108599039
1	245480598	245480599	A	T	21	GENIC	homozygous	108599041
1	245480625	245480626	C	T	24	GENIC	possibly homozygous	108599043
1	245482925	245482926	T	G	26	GENIC	homozygous	108599045
1	245484706	245484707	A	G	31	GENIC	homozygous	108599046
1	245484741	245484742	A	C	33	GENIC	homozygous	108599048
1	245487389	245487390	T	C	22	GENIC	homozygous	108599052
1	245487458	245487459	G	A	30	GENIC	homozygous	108599054
1	245489679	245489680	G	T	26	GENIC	homozygous	108599056
1	245500482	245500483	A	G	34	GENIC	homozygous	108599088
1	245501182	245501183	T	A	25	GENIC	homozygous	108599090
1	245501635	245501636	A	T	30	GENIC	homozygous	108599092
1	245501692	245501693	C	T	27	GENIC	homozygous	120601558
1	245507013	245507014	T	C	32	GENIC	homozygous	108599100
1	245508345	245508346	T	C	39	GENIC	homozygous	108599102
1	245508617	245508618	G	A	28	GENIC	homozygous	108599104
1	245509605	245509606	G	A	20	GENIC	homozygous	108599106
1	245510582	245510583	C	T	20	GENIC	homozygous	108599110
1	245515748	245515749	A	G	29	GENIC	homozygous	108599116
1	245516179	245516180	A	G	38	GENIC	homozygous	108599118