chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	4095918	4095919	C	G	17	GENIC	homozygous	109593584
2	4100353	4100354	C	G	16	GENIC	homozygous	109593585
2	4100397	4100398	G	C	21	GENIC	homozygous	109593586
2	4101081	4101082	G	A	20	GENIC	homozygous	109593587
2	4101112	4101113	C	T	22	GENIC	homozygous	109593588
2	4103291	4103292	T	C	15	GENIC	homozygous	109593589
2	4116348	4116349	C	T	24	GENIC	homozygous	109593604
2	4117539	4117540	C	T	23	GENIC	homozygous	109593605
2	4121633	4121634	C	T	16	GENIC	homozygous	109593606
2	4121988	4121989	G	A	21	GENIC	homozygous	109593607
2	4124871	4124872	C	T	25	GENIC	homozygous	109593608
2	4124914	4124915	C	G	28	GENIC	homozygous	109593609
2	4130354	4130355	C	A	24	GENIC	homozygous	109593610
2	4132551	4132552	G	T	20	GENIC	homozygous	109593612
2	4134189	4134190	G	A	19	GENIC	homozygous	109593613
2	4134276	4134277	G	A	20	GENIC	homozygous	109593614
2	4145748	4145749	G	T	22	GENIC	possibly homozygous	109593623
2	4149246	4149247	T	C	17	GENIC	homozygous	109593625
2	4156811	4156812	C	T	18	GENIC	homozygous	109593630
2	4156824	4156825	C	A	20	GENIC	homozygous	109593631
2	4159311	4159312	A	G	12	GENIC	homozygous	109593632
2	4162331	4162332	T	C	10	GENIC	homozygous	109593633
2	4166414	4166415	T	C	39	GENIC	homozygous	109593634
2	4167093	4167094	C	T	21	GENIC	homozygous	109593635
2	4169701	4169702	C	T	27	GENIC	homozygous	109593638
2	4173383	4173384	G	A	10	GENIC	homozygous	109593639
2	4178160	4178161	T	C	24	GENIC	homozygous	109593641
2	4179859	4179860	G	C	11	GENIC	homozygous	109593643
2	4184980	4184981	G	C	29	GENIC	homozygous	109593644
2	4195748	4195749	T	G	17	GENIC	homozygous	109593645