chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	81889730	81889731	C	CA	38	GENIC	homozygous	60746886
1	81898275	81898276	G	GT	18	GENIC	homozygous	60746888
1	81898284	81898285	T	-	16	GENIC	heterozygous	60746889
1	81898291	81898292	T	C	35	GENIC	possibly homozygous	60746890
1	81898306	81898307	T	C	42	GENIC	heterozygous	60746891
1	81898309	81898310	T	C	42	GENIC	heterozygous	60746892
1	81898316	81898317	T	TC	35	GENIC	possibly homozygous	60746893
1	81898326	81898327	C	CT	32	GENIC	heterozygous	60746894
1	81906191	81906192	G	GTA	22	GENIC	homozygous	60746897
1	81906225	81906226	G	-	23	GENIC	homozygous	60746898
1	81906228	81906229	A	-	23	GENIC	homozygous	60746899
1	81906240	81906241	G	A	28	GENIC	heterozygous	60746900
1	81906259	81906260	A	G	27	GENIC	heterozygous	61448624
1	81907695	81907699	TAAA	----	4	GENIC	homozygous	60746901
1	81908007	81908008	T	TG	30	GENIC	homozygous	60746902
1	81909740	81909742	GT	--	16	GENIC	heterozygous	61448625
1	81910795	81910796	C	CCCCT	25	GENIC	heterozygous	60746904
1	81910819	81910820	G	GA	18	GENIC	heterozygous	60746905
1	81912403	81912404	G	GA	2	GENIC	homozygous	60746906
1	81912405	81912406	G	C	4	GENIC	heterozygous	60746907
1	81920456	81920457	A	G	31	GENIC	heterozygous	61297084