chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91291531	91291532	C	G	25	GENIC	homozygous	117020730
10	91293205	91293206	T	C	22	GENIC	homozygous	117020732
10	91293337	91293338	C	A	27	GENIC	homozygous	117088231
10	91294135	91294136	C	T	39	GENIC	homozygous	117020733
10	91295927	91295928	C	T	30	GENIC	homozygous	117020734
10	91297679	91297680	C	T	8	GENIC	homozygous	117020735
10	91297936	91297937	C	T	20	GENIC	homozygous	117020736
10	91293766	91293767	A	G	28	GENIC	homozygous	116905646
10	91295749	91295750	G	A	42	GENIC	homozygous	116677094
10	91296819	91296820	T	C	27	GENIC	homozygous	116822074
10	91298541	91298542	G	A	12	GENIC	homozygous	117020737
10	91298584	91298585	T	C	12	GENIC	homozygous	117020738
10	91298764	91298765	A	G	22	GENIC	homozygous	116822082
10	91299074	91299075	G	A	16	GENIC	homozygous	117088233
10	91299366	91299367	C	G	25	GENIC	homozygous	116677098
10	91300406	91300407	A	G	21	GENIC	homozygous	116822092
10	91301897	91301898	C	A	18	GENIC	homozygous	116677102