chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49817731	49817732	G	A	34	GENIC	homozygous	117040061
8	49962592	49962593	C	A	23	GENIC	homozygous	116490061
8	49962658	49962659	C	T	27	GENIC	homozygous	116490063
8	49983950	49983951	G	T	19	GENIC	homozygous	116490099
8	49984465	49984466	G	T	28	GENIC	homozygous	116490101
8	49984518	49984519	A	C	27	GENIC	homozygous	116490103
8	49984590	49984591	G	C	30	GENIC	homozygous	117040062
8	49984664	49984665	G	T	34	GENIC	homozygous	116490105
8	50034933	50034934	A	G	39	GENIC	heterozygous	116957774
8	50035651	50035652	T	C	26	GENIC	homozygous	116957778
8	50036332	50036333	G	A	31	GENIC	homozygous	116957780
8	50037999	50038000	T	G	31	GENIC	homozygous	116957782
8	50038713	50038714	T	C	25	GENIC	homozygous	116957784
8	50039344	50039345	A	C	28	GENIC	homozygous	116957786
8	50039390	50039391	G	A	36	GENIC	homozygous	116815018
8	50039469	50039470	A	G	30	GENIC	homozygous	116957788
8	50040304	50040305	G	T	24	GENIC	homozygous	116957790
8	50040496	50040497	C	A	51	GENIC	homozygous	116815020
8	50041614	50041615	T	G	62	GENIC	homozygous	117040063
8	50041615	50041616	T	A	61	GENIC	homozygous	117040064
8	50041774	50041775	T	A	53	GENIC	possibly homozygous	116957792
8	50045170	50045171	T	G	43	GENIC	homozygous	116815026
8	50045806	50045807	G	A	20	GENIC	homozygous	116815028
8	50046227	50046228	G	A	37	GENIC	possibly homozygous	116957800
8	50046486	50046487	G	C	34	GENIC	homozygous	116957802
8	50046575	50046576	C	A	50	GENIC	homozygous	116815034
8	50046796	50046797	G	A	30	GENIC	homozygous	116957804
8	50046889	50046890	T	C	30	GENIC	homozygous	116957806
8	50049425	50049426	C	T	29	GENIC	possibly homozygous	116957808
8	50053702	50053703	G	A	15	GENIC	homozygous	116957810