chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10775101	10775102	G	A	19	GENIC	homozygous	116493695
10	10775351	10775352	T	C	13	GENIC	homozygous	116493697
10	10776154	10776155	A	G	18	GENIC	homozygous	116493699
10	10776268	10776269	C	T	21	GENIC	homozygous	116493701
10	10776837	10776838	C	T	26	GENIC	homozygous	116493703
10	10777390	10777391	C	T	31	GENIC	homozygous	116493705
10	10777433	10777434	G	A	23	GENIC	homozygous	116493707
10	10778194	10778195	T	G	19	GENIC	homozygous	116493709
10	10778196	10778197	G	T	19	GENIC	homozygous	116493711
10	10779448	10779449	A	G	28	GENIC	homozygous	116493713
10	10780382	10780383	G	A	15	GENIC	homozygous	116493717
10	10780412	10780413	T	A	14	GENIC	homozygous	116493719
10	10780413	10780414	C	A	16	GENIC	homozygous	116493721
10	10782736	10782737	T	C	10	GENIC	homozygous	116493723
10	10782804	10782805	G	A	19	GENIC	homozygous	116493725
10	10783067	10783068	G	T	29	GENIC	homozygous	116734080
10	10784266	10784267	G	A	31	GENIC	homozygous	116734081