chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	142504023	142504024	C	G	9	GENIC	possibly homozygous	74855723
2	142504027	142504028	C	G	7	GENIC	heterozygous	74855726
2	142504031	142504032	C	G	5	GENIC	heterozygous	74855729
2	142504039	142504040	A	C	5	GENIC	heterozygous	78698595
2	142504041	142504042	C	A	5	GENIC	heterozygous	78698596
2	142504043	142504044	A	C	5	GENIC	heterozygous	78698597
2	142504051	142504052	A	C	4	GENIC	heterozygous	78698598
2	142504425	142504426	T	C	12	GENIC	homozygous	74855732
2	142504541	142504542	G	A	30	GENIC	homozygous	74855735
2	142505295	142505296	T	G	50	GENIC	heterozygous	74855750
2	142505949	142505950	C	T	36	GENIC	homozygous	74855756
2	142508149	142508150	G	A	31	GENIC	homozygous	74855759
2	142508222	142508223	G	A	26	GENIC	homozygous	74855762
2	142509162	142509163	G	C	14	GENIC	homozygous	74855765
2	142509278	142509279	T	C	13	GENIC	heterozygous	74855768
2	142509319	142509320	T	C	11	GENIC	heterozygous	78698599
2	142509322	142509323	T	C	11	GENIC	heterozygous	78698600
2	142509400	142509401	C	T	9	GENIC	possibly homozygous	74855777
2	142509531	142509532	G	A	28	GENIC	homozygous	74855780
2	142509779	142509780	G	A	30	GENIC	homozygous	74855783
2	142509939	142509940	G	A	14	GENIC	homozygous	74855786
2	142510087	142510088	C	G	22	GENIC	homozygous	74855795
2	142510355	142510356	C	A	20	GENIC	homozygous	74855801