chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	174361309	174361310	A	C	85	GENIC	heterozygous	108391572
1	174361340	174361341	C	A	107	GENIC	heterozygous	108391574
1	174361919	174361920	C	T	34	GENIC	homozygous	108391576
1	174362540	174362541	T	C	53	GENIC	homozygous	108391578
1	174362993	174362994	C	T	29	GENIC	homozygous	108391580
1	174363653	174363654	A	G	56	GENIC	homozygous	108391582
1	174364155	174364156	A	G	62	GENIC	homozygous	108391584
1	174364177	174364178	T	C	90	GENIC	heterozygous	108391586
1	174364219	174364220	T	C	115	GENIC	heterozygous	108391588
1	174364235	174364236	T	C	105	GENIC	heterozygous	108391590
1	174364248	174364249	C	T	86	GENIC	heterozygous	108391592
1	174365180	174365181	T	C	22	GENIC	homozygous	108391594
1	174367804	174367805	A	G	28	GENIC	homozygous	108391596
1	174368309	174368310	T	C	31	GENIC	homozygous	108391598
1	174369065	174369066	T	C	46	GENIC	homozygous	108391600
1	174370317	174370318	A	T	56	GENIC	homozygous	108391602
1	174372435	174372436	A	G	39	GENIC	homozygous	108391604
1	174372505	174372506	T	C	51	GENIC	possibly homozygous	108391606
1	174374374	174374375	T	G	39	GENIC	homozygous	108391608
1	174374894	174374895	C	T	38	GENIC	homozygous	108391610
1	174375404	174375405	A	C	27	GENIC	homozygous	108391612
1	174375710	174375711	A	C	34	GENIC	homozygous	108391614
1	174376017	174376018	G	A	47	GENIC	homozygous	108391616
1	174376566	174376567	C	T	42	GENIC	possibly homozygous	108391618
1	174377096	174377097	A	T	22	GENIC	homozygous	108391620
1	174378345	174378346	T	C	37	GENIC	homozygous	108391622
1	174379976	174379977	T	C	24	GENIC	homozygous	108391624