chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3829967	3829968	T	C	29	GENIC	homozygous	109070093
20	3830001	3830002	T	C	22	GENIC	homozygous	109070095
20	3830339	3830340	T	C	43	GENIC	homozygous	109070099
20	3830615	3830616	A	G	38	GENIC	homozygous	109070101
20	3831037	3831038	C	T	18	GENIC	homozygous	109070103
20	3832085	3832086	A	G	25	GENIC	homozygous	109070105
20	3832428	3832429	C	T	44	GENIC	homozygous	109070107
20	3833107	3833108	G	T	39	GENIC	possibly homozygous	109417533
20	3833188	3833189	T	C	36	GENIC	homozygous	109070109
20	3849395	3849396	C	T	20	GENIC	homozygous	109070113
20	3849766	3849767	C	T	30	GENIC	homozygous	109070115
20	3850907	3850908	C	T	30	GENIC	homozygous	109070117
20	3851160	3851161	G	A	19	GENIC	homozygous	109070119
20	3851319	3851320	C	T	14	GENIC	homozygous	109070121
20	3851678	3851679	T	C	20	GENIC	homozygous	109417535
20	3852383	3852384	G	A	22	GENIC	homozygous	109070127
20	3852989	3852990	A	G	42	GENIC	homozygous	109070129
20	3853012	3853013	G	T	39	GENIC	possibly homozygous	109070131
20	3853057	3853058	G	A	30	GENIC	homozygous	109070133
20	3854106	3854107	G	A	35	GENIC	homozygous	109070135
20	3854492	3854493	A	G	39	GENIC	homozygous	109070139
20	3855518	3855519	G	A	27	GENIC	homozygous	109417537
20	3856428	3856429	C	T	29	GENIC	homozygous	109417539