chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91291531	91291532	C	G	32	GENIC	homozygous	117020730
10	91293205	91293206	T	C	42	GENIC	homozygous	117020732
10	91293337	91293338	C	A	50	GENIC	homozygous	117088231
10	91293766	91293767	A	G	45	GENIC	homozygous	116905646
10	91294135	91294136	C	T	51	GENIC	possibly homozygous	117020733
10	91295749	91295750	G	A	75	GENIC	possibly homozygous	116677094
10	91295927	91295928	C	T	55	GENIC	homozygous	117020734
10	91296819	91296820	T	C	37	GENIC	homozygous	116822074
10	91297679	91297680	C	T	31	GENIC	homozygous	117020735
10	91297936	91297937	C	T	42	GENIC	homozygous	117020736
10	91298541	91298542	G	A	37	GENIC	homozygous	117020737
10	91298584	91298585	T	C	41	GENIC	homozygous	117020738
10	91298764	91298765	A	G	53	GENIC	homozygous	116822082
10	91299074	91299075	G	A	43	GENIC	homozygous	117088233
10	91299366	91299367	C	G	56	GENIC	possibly homozygous	116677098
10	91300406	91300407	A	G	50	GENIC	homozygous	116822092
10	91301897	91301898	C	A	38	GENIC	homozygous	116677102