chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89685102	89685103	G	A	36	GENIC	homozygous	116820857
10	89685974	89685975	T	C	29	GENIC	homozygous	116820859
10	89687468	89687469	A	T	43	GENIC	homozygous	116820861
10	89687531	89687532	C	T	39	GENIC	homozygous	116820863
10	89687532	89687533	A	G	38	GENIC	homozygous	116820865
10	89687683	89687684	G	C	23	GENIC	homozygous	116820867
10	89688154	89688155	A	G	19	GENIC	homozygous	116820869
10	89688635	89688636	T	C	30	GENIC	homozygous	116820871
10	89689267	89689268	T	C	41	GENIC	homozygous	117173796
10	89689442	89689443	T	C	31	GENIC	homozygous	116820873
10	89690317	89690318	A	G	36	GENIC	homozygous	116820875
10	89692605	89692606	G	A	46	GENIC	homozygous	116820877
10	89692644	89692645	G	A	51	GENIC	possibly homozygous	116820879
10	89692684	89692685	C	T	39	GENIC	homozygous	116820881
10	89692944	89692945	G	A	29	GENIC	homozygous	116820883
10	89694196	89694197	C	A	28	GENIC	homozygous	116820887
10	89694292	89694293	A	G	20	GENIC	homozygous	117328708
10	89694338	89694339	G	A	25	GENIC	homozygous	118107475
10	89694581	89694582	T	C	29	GENIC	homozygous	116820891
10	89695856	89695857	T	C	42	GENIC	homozygous	116820893
10	89696412	89696413	A	G	38	GENIC	homozygous	116820895
10	89697257	89697258	G	A	27	GENIC	homozygous	116820897
10	89697484	89697485	T	C	33	GENIC	homozygous	116902944
10	89699360	89699361	A	G	11	GENIC	homozygous	116675738
10	89699369	89699370	C	G	8	GENIC	homozygous	116675740
10	89699371	89699372	C	G	6	GENIC	homozygous	116675742