chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	36296229	36296230	C	A	29	GENIC	homozygous	108075907
1	36297833	36297834	C	T	27	GENIC	homozygous	109475590
1	36298371	36298372	A	G	43	GENIC	homozygous	109475591
1	36299322	36299323	G	A	37	GENIC	homozygous	108075926
1	36299340	36299341	C	T	42	GENIC	possibly homozygous	109475592
1	36299606	36299607	T	C	28	GENIC	homozygous	109475593
1	36299608	36299609	G	C	27	GENIC	homozygous	109475594
1	36300052	36300053	C	A	31	GENIC	homozygous	109475595
1	36301514	36301515	T	C	43	GENIC	homozygous	108075935
1	36301611	36301612	A	G	46	GENIC	homozygous	108075937
1	36301684	36301685	T	C	43	GENIC	homozygous	109475596
1	36306562	36306563	G	A	39	GENIC	homozygous	109475597
1	36306787	36306788	C	T	44	GENIC	homozygous	109475598
1	36308604	36308605	T	C	16	GENIC	homozygous	108075978
1	36308719	36308720	A	T	19	GENIC	homozygous	108075980
1	36309666	36309667	A	G	38	GENIC	homozygous	108075989
1	36314101	36314102	G	C	29	GENIC	homozygous	109475599