chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170621280	170621281	G	A	17	GENIC	heterozygous	61960434
1	170622094	170622095	C	T	8	GENIC	heterozygous	62785703
1	170622756	170622757	T	C	10	GENIC	homozygous	60941111
1	170623122	170623123	C	A	12	GENIC	homozygous	60941112
1	170623538	170623539	A	G	20	GENIC	heterozygous	61960435
1	170623869	170623870	G	A	18	GENIC	heterozygous	61960436
1	170624310	170624311	C	A	8	GENIC	heterozygous	61960438
1	170624902	170624903	C	A	7	GENIC	heterozygous	61960441
1	170625066	170625067	C	A	6	GENIC	heterozygous	61960442
1	170625101	170625102	G	A	8	GENIC	heterozygous	61909301
1	170625107	170625108	G	A	9	GENIC	heterozygous	61960443
1	170625345	170625346	G	A	11	GENIC	heterozygous	61909302
1	170628280	170628281	G	A	10	GENIC	heterozygous	61909304
1	170628709	170628710	A	G	13	GENIC	homozygous	60941115
1	170628777	170628778	T	C	12	GENIC	heterozygous	61960445
1	170629089	170629092	AAC	---	8	GENIC	heterozygous	62785704
1	170629637	170629638	G	A	15	GENIC	homozygous	60941117
1	170631445	170631446	T	C	13	GENIC	homozygous	60941118
1	170631481	170631482	C	-	9	GENIC	heterozygous	60941120
1	170631487	170631488	A	C	11	GENIC	heterozygous	62173313
1	170632111	170632112	C	T	16	GENIC	heterozygous	61960446
1	170632202	170632203	T	C	14	GENIC	homozygous	60941121
1	170632494	170632496	AG	--	9	GENIC	heterozygous	62785705
1	170632498	170632499	G	-	9	GENIC	heterozygous	62785706
1	170632500	170632504	CTTG	----	9	GENIC	heterozygous	62785707