chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	24189342	24189343	C	A	22	GENIC	possibly homozygous	109553743
1	24218648	24218649	T	C	23	GENIC	possibly homozygous	108056616
1	24220350	24220351	C	T	37	GENIC	homozygous	109472294
1	24223897	24223898	C	T	19	GENIC	heterozygous	108056625
1	24248873	24248874	C	A	20	GENIC	homozygous	108056647
1	24275742	24275743	A	C	21	GENIC	homozygous	108056668
1	24275812	24275813	A	G	27	GENIC	homozygous	108056669
1	24295151	24295152	G	T	28	GENIC	possibly homozygous	108056672
1	24295359	24295360	G	T	22	GENIC	homozygous	108056673
1	24295419	24295420	G	C	24	GENIC	homozygous	108056674
1	24295515	24295516	A	T	22	GENIC	homozygous	108056675
1	24295692	24295693	G	C	34	GENIC	homozygous	108056676
1	24295764	24295765	T	G	31	GENIC	homozygous	108056677
1	24295770	24295771	C	G	24	GENIC	homozygous	108056678
1	24295773	24295774	T	G	23	GENIC	homozygous	108056679
1	24295785	24295786	G	T	31	GENIC	homozygous	108056680
1	24295796	24295797	T	G	32	GENIC	homozygous	108056681
1	24295825	24295826	T	A	31	GENIC	homozygous	108056682
1	24295895	24295896	C	A	18	GENIC	homozygous	108056683
1	24297737	24297738	A	C	27	GENIC	homozygous	108056686
1	24297739	24297740	T	C	27	GENIC	homozygous	108056687
1	24297755	24297756	T	C	27	GENIC	homozygous	108056688