chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3553817	3553818	A	G	30	GENIC	homozygous	109388986
20	3553853	3553854	C	T	21	GENIC	homozygous	109388987
20	3554097	3554098	T	G	21	GENIC	homozygous	109069052
20	3554158	3554159	A	C	20	GENIC	homozygous	109388988
20	3554221	3554222	T	C	24	GENIC	homozygous	109388989
20	3554222	3554223	G	T	24	GENIC	homozygous	109388990
20	3554389	3554390	C	T	20	GENIC	homozygous	109388991
20	3554522	3554523	C	T	18	GENIC	homozygous	109388992
20	3555186	3555187	G	A	15	GENIC	homozygous	109388993
20	3557381	3557382	G	T	11	GENIC	homozygous	109388994
20	3557933	3557934	C	A	26	GENIC	homozygous	109388995
20	3558080	3558081	T	C	27	GENIC	homozygous	109069062
20	3559601	3559602	G	A	27	GENIC	homozygous	109388996
20	3559779	3559780	C	A	31	GENIC	homozygous	109388997
20	3561391	3561392	A	G	31	GENIC	homozygous	109069070
20	3563239	3563240	T	A	24	GENIC	homozygous	109231770
20	3563287	3563288	C	T	33	GENIC	homozygous	109388998
20	3564101	3564102	C	A	28	GENIC	homozygous	109388999
20	3564277	3564278	C	A	36	GENIC	homozygous	109389000
20	3564434	3564435	T	C	32	GENIC	homozygous	109069076
20	3565917	3565918	C	T	48	GENIC	homozygous	109231771
20	3567225	3567226	G	A	19	GENIC	homozygous	109389001
20	3568323	3568324	T	G	18	GENIC	homozygous	109069084
20	3570271	3570272	T	C	24	GENIC	homozygous	109069086
20	3571676	3571677	T	C	17	GENIC	homozygous	109389002
20	3571713	3571714	G	T	13	GENIC	homozygous	109389003
20	3572048	3572049	T	C	16	GENIC	homozygous	109389004
20	3573009	3573010	T	G	25	GENIC	homozygous	109069090
20	3573647	3573648	G	A	17	GENIC	homozygous	109069095
20	3574144	3574145	G	C	12	GENIC	homozygous	109389005