chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	165086045	165086046	C	T	28	GENIC	homozygous	109435815
1	165087042	165087043	G	T	38	GENIC	homozygous	109435817
1	165087665	165087666	A	G	19	GENIC	homozygous	108352584
1	165088711	165088712	A	G	27	GENIC	homozygous	108352586
1	165088760	165088761	T	A	25	GENIC	homozygous	109435819
1	165089070	165089071	C	T	21	GENIC	homozygous	109435821
1	165092824	165092825	T	C	25	GENIC	homozygous	109435823
1	165093119	165093120	C	G	32	GENIC	homozygous	109435825
1	165094021	165094022	T	C	27	GENIC	homozygous	109435827
1	165097759	165097760	C	A	31	GENIC	homozygous	109435829
1	165098704	165098705	C	T	22	GENIC	homozygous	109435831
1	165101384	165101385	C	T	24	GENIC	homozygous	109435833
1	165106497	165106498	G	A	18	GENIC	homozygous	109435835
1	165106567	165106568	G	A	29	GENIC	homozygous	109435837
1	165111583	165111584	C	T	36	GENIC	homozygous	108352646
1	165111592	165111593	G	A	35	GENIC	homozygous	109435841
1	165115626	165115627	A	G	28	GENIC	homozygous	108352658
1	165115959	165115960	G	A	32	GENIC	homozygous	109435843
1	165116040	165116041	G	A	30	GENIC	homozygous	108352662
1	165116065	165116066	T	C	26	GENIC	homozygous	108352664
1	165116501	165116502	T	A	17	GENIC	homozygous	109435845
1	165118851	165118852	A	G	36	GENIC	homozygous	108352673
1	165119180	165119181	T	G	22	GENIC	homozygous	109435847
1	165120883	165120884	A	C	22	GENIC	homozygous	108954098
1	165121560	165121561	G	A	23	GENIC	homozygous	109435849