chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10775101	10775102	G	A	30	GENIC	homozygous	116493695
10	10775351	10775352	T	C	33	GENIC	homozygous	116493697
10	10776154	10776155	A	G	65	GENIC	homozygous	116493699
10	10776268	10776269	C	T	32	GENIC	homozygous	116493701
10	10776837	10776838	C	T	44	GENIC	homozygous	116493703
10	10777390	10777391	C	T	33	GENIC	homozygous	116493705
10	10777433	10777434	G	A	36	GENIC	homozygous	116493707
10	10778194	10778195	T	G	7	GENIC	homozygous	116493709
10	10778196	10778197	G	T	7	GENIC	homozygous	116493711
10	10779448	10779449	A	G	39	GENIC	homozygous	116493713
10	10780382	10780383	G	A	46	GENIC	homozygous	116493717
10	10780412	10780413	T	A	34	GENIC	homozygous	116493719
10	10780413	10780414	C	A	34	GENIC	homozygous	116493721
10	10781612	10781613	T	C	41	GENIC	homozygous	116993885
10	10782736	10782737	T	C	49	GENIC	homozygous	116493723
10	10782804	10782805	G	A	46	GENIC	homozygous	116493725
10	10784074	10784075	A	G	42	GENIC	homozygous	116493729
10	10784176	10784177	G	A	47	GENIC	homozygous	116993886