chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	151565213	151565214	A	G	37	GENIC	homozygous	111777718
3	151566594	151566595	G	A	30	GENIC	homozygous	112310773
3	151567986	151567987	C	T	21	GENIC	homozygous	111777720
3	151569189	151569190	T	C	11	GENIC	homozygous	111777722
3	151569216	151569217	G	A	19	GENIC	homozygous	112310775
3	151569564	151569565	C	A	28	GENIC	possibly homozygous	112310777
3	151569833	151569834	T	C	28	GENIC	possibly homozygous	111777724
3	151569893	151569894	A	G	23	GENIC	possibly homozygous	111777726
3	151570874	151570875	T	C	17	GENIC	homozygous	111777728
3	151571723	151571724	C	T	28	GENIC	heterozygous	112310779
3	151573651	151573652	C	T	27	GENIC	homozygous	111777730
3	151575803	151575804	G	A	25	GENIC	homozygous	112310781
3	151580014	151580015	G	A	29	GENIC	homozygous	111777736
3	151580053	151580054	C	T	31	GENIC	possibly homozygous	111777738
3	151580079	151580080	G	A	62	GENIC	heterozygous	111777740
3	151580129	151580130	G	A	78	GENIC	heterozygous	112310783
3	151581224	151581225	A	C	20	GENIC	homozygous	111777742
3	151583542	151583543	T	A	17	GENIC	homozygous	112310785