chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91295727	91295728	C	T	28	GENIC	homozygous	116951866
10	91295749	91295750	G	A	32	GENIC	homozygous	116677094
10	91295809	91295810	A	G	26	GENIC	homozygous	116822068
10	91295815	91295816	G	A	31	GENIC	possibly homozygous	116822070
10	91296122	91296123	G	A	42	GENIC	homozygous	116822072
10	91296819	91296820	T	C	44	GENIC	homozygous	116822074
10	91298134	91298135	T	C	55	GENIC	homozygous	116822076
10	91298547	91298548	G	A	30	GENIC	homozygous	116951868
10	91298637	91298638	C	T	51	GENIC	homozygous	116822078
10	91298704	91298705	G	A	38	GENIC	homozygous	116822080
10	91298764	91298765	A	G	49	GENIC	homozygous	116822082
10	91299097	91299098	G	A	33	GENIC	homozygous	116822084
10	91299366	91299367	C	G	32	GENIC	homozygous	116677098
10	91299615	91299616	A	C	41	GENIC	possibly homozygous	116822086
10	91300054	91300055	A	G	39	GENIC	possibly homozygous	116822088
10	91300067	91300068	G	A	40	GENIC	possibly homozygous	116822090
10	91301884	91301885	A	G	30	GENIC	homozygous	116677100
10	91301897	91301898	C	A	29	GENIC	homozygous	116677102