chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	81889730	81889731	C	CA	21	GENIC	homozygous	60746886
1	81891276	81891277	C	A	28	GENIC	heterozygous	60746887
1	81898275	81898276	G	GT	14	GENIC	homozygous	60746888
1	81898284	81898285	T	-	17	GENIC	possibly homozygous	60746889
1	81898291	81898292	T	C	37	GENIC	possibly homozygous	60746890
1	81898306	81898307	T	C	37	GENIC	heterozygous	60746891
1	81898309	81898310	T	C	37	GENIC	heterozygous	60746892
1	81898316	81898317	T	TC	32	GENIC	possibly homozygous	60746893
1	81898326	81898327	C	CT	31	GENIC	heterozygous	60746894
1	81906191	81906192	G	-	19	GENIC	heterozygous	60746896
1	81906191	81906192	G	GTA	19	GENIC	homozygous	60746897
1	81906225	81906226	G	-	13	GENIC	homozygous	60746898
1	81906228	81906229	A	-	14	GENIC	possibly homozygous	60746899
1	81906240	81906241	G	A	20	GENIC	heterozygous	60746900
1	81906259	81906260	A	G	22	GENIC	heterozygous	61448624
1	81907695	81907699	TAAA	----	8	GENIC	homozygous	60746901
1	81908007	81908008	T	TG	18	GENIC	homozygous	60746902
1	81909740	81909742	GT	--	7	GENIC	heterozygous	61448625
1	81910791	81910792	C	T	28	GENIC	heterozygous	60746903
1	81910795	81910796	C	CCCCT	21	GENIC	heterozygous	60746904
1	81910819	81910820	G	GA	24	GENIC	heterozygous	60746905
1	81912403	81912404	G	GA	2	GENIC	homozygous	60746906
1	81912405	81912406	G	C	4	GENIC	homozygous	60746907
1	81920456	81920457	A	G	29	GENIC	heterozygous	61297084