chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50979719	50979720	A	G	58	GENIC	homozygous	138329685
8	50980135	50980136	C	T	73	GENIC	homozygous	138329686
8	50981010	50981010		A	55	GENIC	possibly homozygous	138244863
8	50981539	50981540	G	C	58	GENIC	homozygous	138329687
8	50981663	50981664	T	A	58	GENIC	homozygous	138329688
8	50981860	50981861	T	C	47	GENIC	homozygous	138329689
8	50983266	50983267	A	G	52	GENIC	homozygous	138329690
8	50983869	50983870	C	T	21	GENIC	homozygous	138329691
8	50984413	50984414	T	C	38	GENIC	homozygous	138329692
8	50989252	50989253	A	C	52	GENIC	homozygous	138329693
8	50991473	50991474	G	A	61	GENIC	homozygous	138329694
8	50992266	50992267	C		67	GENIC	homozygous	138244864
8	50992267	50992268	C	T	69	GENIC	homozygous	138329695
8	50992439	50992440	C	G	58	GENIC	homozygous	138329696
8	50993580	50993581	T	A	51	GENIC	homozygous	138329697
8	50996221	50996222	C	T	23	GENIC	homozygous	138329698
8	50997824	50997825	A	T	59	GENIC	homozygous	138329699
8	50998519	50998520	G	A	54	GENIC	homozygous	138329700
8	50998931	50998931		TCC	52	GENIC	possibly homozygous	138244865
8	50999666	50999667	G	A	51	GENIC	homozygous	138329701
8	51001033	51001033		TG	35	GENIC	homozygous	138244866
8	51001077	51001077		TG	32	GENIC	homozygous	138244867
8	51002590	51002591	C	A	35	GENIC	heterozygous	403237545
8	50996251	50996252	C	T	39	GENIC	possibly homozygous	154518244
8	50996251	50996252	C		39	GENIC	heterozygous	403237543
8	51002590	51002591	C		35	GENIC	possibly homozygous	403237544