chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	143802738	143802739	A	G	27	GENIC	homozygous	108267115
1	143803988	143803989	G	A	28	GENIC	homozygous	108267117
1	143805378	143805379	T	C	19	GENIC	homozygous	108267121
1	143805491	143805492	G	A	21	GENIC	homozygous	108267123
1	143805665	143805666	G	A	20	GENIC	homozygous	109050646
1	143806715	143806716	A	G	44	GENIC	homozygous	108267125
1	143806970	143806971	A	G	39	GENIC	homozygous	108267127
1	143807352	143807353	T	C	24	GENIC	homozygous	108267129
1	143808237	143808238	T	C	30	GENIC	homozygous	108267131
1	143809249	143809250	G	A	39	GENIC	homozygous	109328682
1	143810173	143810174	A	G	38	GENIC	homozygous	108267133
1	143810233	143810234	T	C	39	GENIC	homozygous	108267135
1	143810993	143810994	C	T	39	GENIC	homozygous	109050650
1	143811520	143811521	A	G	28	GENIC	homozygous	108267137
1	143814892	143814893	G	T	16	GENIC	homozygous	109328684
1	143815851	143815852	C	A	20	GENIC	homozygous	108267143
1	143815860	143815861	C	T	22	GENIC	homozygous	109328686
1	143817992	143817993	T	C	19	GENIC	homozygous	109050655