chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89655290	89655291	G	A	78	GENIC	heterozygous	118007614
10	89657652	89657653	T	G	32	GENIC	heterozygous	118007615
10	89659549	89659550	A	G	34	GENIC	heterozygous	118007616
10	89659555	89659556	T	C	37	GENIC	heterozygous	118007617
10	89659561	89659562	T	C	38	GENIC	heterozygous	118007618
10	89659650	89659651	T	A	54	GENIC	heterozygous	118007619
10	89660875	89660876	G	A	31	GENIC	heterozygous	118007620
10	89669133	89669134	A	T	43	GENIC	homozygous	116675730
10	89669161	89669162	A	G	35	GENIC	homozygous	116820771
10	89669196	89669197	G	T	31	GENIC	homozygous	118007621
10	89669226	89669227	T	C	21	GENIC	homozygous	118007622
10	89669230	89669231	G	T	22	GENIC	homozygous	118007623
10	89669250	89669251	G	T	19	GENIC	homozygous	116675732
10	89669252	89669253	G	T	18	GENIC	homozygous	118007624
10	89669254	89669255	G	T	18	GENIC	homozygous	118007625
10	89669256	89669257	A	T	18	GENIC	homozygous	118007626
10	89669260	89669261	C	T	18	GENIC	homozygous	116675734
10	89669345	89669346	A	G	19	GENIC	homozygous	117105234
10	89678144	89678145	C	T	38	GENIC	possibly homozygous	116675736