chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	142504023	142504024	C	G	7	GENIC	heterozygous	74855723
2	142504425	142504426	T	C	2	GENIC	homozygous	74855732
2	142504541	142504542	G	A	28	GENIC	homozygous	74855735
2	142505071	142505072	G	A	47	GENIC	possibly homozygous	74855738
2	142505090	142505091	G	A	26	GENIC	heterozygous	74855741
2	142505284	142505285	A	G	76	GENIC	heterozygous	74855747
2	142505295	142505296	T	G	75	GENIC	heterozygous	74855750
2	142505314	142505315	G	T	62	GENIC	heterozygous	74855753
2	142505949	142505950	C	T	42	GENIC	homozygous	74855756
2	142508149	142508150	G	A	44	GENIC	homozygous	74855759
2	142508222	142508223	G	A	31	GENIC	homozygous	74855762
2	142509162	142509163	G	C	23	GENIC	homozygous	74855765
2	142509278	142509279	T	C	15	GENIC	possibly homozygous	74855768
2	142509335	142509336	C	T	9	GENIC	heterozygous	74855771
2	142509386	142509387	T	C	16	GENIC	heterozygous	74855774
2	142509400	142509401	C	T	20	GENIC	heterozygous	74855777
2	142509531	142509532	G	A	27	GENIC	homozygous	74855780
2	142509779	142509780	G	A	50	GENIC	possibly homozygous	74855783
2	142509939	142509940	G	A	17	GENIC	homozygous	74855786
2	142509953	142509954	G	A	13	GENIC	heterozygous	74855789
2	142510087	142510088	C	G	41	GENIC	homozygous	74855795
2	142510355	142510356	C	A	22	GENIC	homozygous	74855801