chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	77848816	77848817	C	G	16	GENIC	homozygous	108871828
1	77848928	77848929	T	C	33	GENIC	homozygous	108871829
1	77850449	77850450	C	T	23	GENIC	homozygous	108871830
1	77850709	77850710	T	A	27	GENIC	homozygous	108871831
1	77850951	77850952	A	G	19	GENIC	homozygous	108871832
1	77851498	77851499	C	T	29	GENIC	possibly homozygous	108871833
1	77851722	77851723	G	A	29	GENIC	homozygous	108871834
1	77851809	77851810	G	T	29	GENIC	heterozygous	108871836
1	77853156	77853157	G	A	35	GENIC	homozygous	108871837
1	77853172	77853173	T	C	31	GENIC	homozygous	108871838
1	77855363	77855364	C	T	37	GENIC	homozygous	108871839
1	77855998	77855999	C	T	25	GENIC	homozygous	108871840
1	77856415	77856416	T	C	26	GENIC	homozygous	108871841
1	77856734	77856735	T	C	27	GENIC	homozygous	108871842
1	77856753	77856754	A	G	31	GENIC	homozygous	108871843
1	77856942	77856943	C	T	19	GENIC	homozygous	108871844
1	77857122	77857123	T	C	15	GENIC	heterozygous	108871845
1	77858650	77858651	A	G	36	GENIC	homozygous	108871846
1	77859487	77859488	G	A	38	GENIC	homozygous	108871847
1	77859594	77859595	G	A	36	GENIC	heterozygous	108871848
1	77859642	77859643	C	A	41	GENIC	heterozygous	108871849
1	77859662	77859663	C	T	39	GENIC	heterozygous	108871850
1	77860784	77860785	T	C	29	GENIC	homozygous	108871851
1	77860991	77860992	T	C	25	GENIC	homozygous	108871852
1	77862388	77862389	A	G	19	GENIC	homozygous	108871853
1	77863131	77863132	G	T	24	GENIC	homozygous	108871854
1	77864705	77864706	T	G	21	GENIC	homozygous	108871855
1	77865705	77865706	G	A	27	GENIC	homozygous	108871856