chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	162370053	162370054	G	C	55	GENIC	homozygous	108344449
1	162371170	162371171	A	T	44	GENIC	homozygous	108344451
1	162372300	162372301	A	G	59	GENIC	homozygous	108344453
1	162372421	162372422	G	A	62	GENIC	homozygous	108344455
1	162372501	162372502	C	T	44	GENIC	homozygous	108344457
1	162372880	162372881	A	C	53	GENIC	homozygous	108344459
1	162373507	162373508	A	G	46	GENIC	homozygous	108344461
1	162373838	162373839	A	T	42	GENIC	homozygous	108344463
1	162373987	162373988	A	G	49	GENIC	homozygous	108344465
1	162374382	162374383	T	C	50	GENIC	homozygous	108344467
1	162374592	162374593	C	G	46	GENIC	homozygous	108344469
1	162374767	162374768	G	A	39	GENIC	homozygous	108344471
1	162374819	162374820	C	T	41	GENIC	homozygous	108751116
1	162374820	162374821	T	G	41	GENIC	homozygous	108751117
1	162374912	162374913	C	G	31	GENIC	homozygous	108344473
1	162374945	162374946	G	A	29	GENIC	homozygous	108344475
1	162374966	162374967	A	G	25	GENIC	homozygous	108344477
1	162375025	162375026	A	G	28	GENIC	homozygous	108344479
1	162375342	162375343	A	G	40	GENIC	homozygous	108344481
1	162375363	162375364	G	A	39	GENIC	homozygous	108751118
1	162375364	162375365	A	C	40	GENIC	homozygous	108751119
1	162375683	162375684	T	C	50	GENIC	homozygous	108344483
1	162373615	162373616	T		39	GENIC	homozygous	127451448
1	162373097	162373097		GTTG	44	GENIC	homozygous	127451447