chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10775101	10775102	G	A	25	GENIC	homozygous	116493695
10	10775351	10775352	T	C	18	GENIC	homozygous	116493697
10	10775701	10775701		TTTTG	14	GENIC	homozygous	131087101
10	10776154	10776155	A	G	22	GENIC	homozygous	116493699
10	10776268	10776269	C	T	17	GENIC	homozygous	116493701
10	10776837	10776838	C	T	21	GENIC	homozygous	116493703
10	10777390	10777391	C	T	24	GENIC	homozygous	116493705
10	10777433	10777434	G	A	21	GENIC	homozygous	116493707
10	10778194	10778195	T	G	12	GENIC	homozygous	116493709
10	10778196	10778197	G	T	12	GENIC	homozygous	116493711
10	10779448	10779449	A	G	29	GENIC	homozygous	116493713
10	10779706	10779707	C	T	17	GENIC	homozygous	117102508
10	10779804	10779805	G	A	19	GENIC	homozygous	116493715
10	10780292	10780294	CT		16	GENIC	homozygous	128789529
10	10780307	10780309	AT		14	GENIC	homozygous	128789530
10	10780382	10780383	G	A	27	GENIC	homozygous	116493717
10	10780412	10780413	T	A	23	GENIC	homozygous	116493719
10	10780413	10780414	C	A	23	GENIC	homozygous	116493721
10	10782736	10782737	T	C	16	GENIC	homozygous	116493723
10	10782804	10782805	G	A	21	GENIC	homozygous	116493725
10	10784266	10784267	G	A	19	GENIC	homozygous	116734081
10	10779719	10779720	C	T	15	GENIC	homozygous	117140125
10	10780296	10780297	C	T	16	GENIC	homozygous	117119890
10	10783067	10783068	G	T	13	GENIC	possibly homozygous	116734080