chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10775101	10775102	G	A	28	GENIC	homozygous	116493695
10	10775351	10775352	T	C	20	GENIC	homozygous	116493697
10	10775701	10775701		TTTTG	20	GENIC	homozygous	131087101
10	10776154	10776155	A	G	26	GENIC	homozygous	116493699
10	10776268	10776269	C	T	22	GENIC	homozygous	116493701
10	10776837	10776838	C	T	25	GENIC	homozygous	116493703
10	10777390	10777391	C	T	29	GENIC	homozygous	116493705
10	10777433	10777434	G	A	21	GENIC	homozygous	116493707
10	10778194	10778195	T	G	31	GENIC	possibly homozygous	116493709
10	10778196	10778197	G	T	32	GENIC	homozygous	116493711
10	10778382	10778384	AC		13	GENIC	homozygous	128789527
10	10778558	10778558		AC	4	GENIC	homozygous	131087103
10	10778650	10778652	AC		14	GENIC	homozygous	131087104
10	10778639	10778640	T	C	15	GENIC	homozygous	118026515
10	10778579	10778580	T	C	10	GENIC	homozygous	117981154
10	10778631	10778632	C	T	14	GENIC	homozygous	131099869
10	10778633	10778634	T	C	15	GENIC	homozygous	131099870
10	10779448	10779449	A	G	30	GENIC	homozygous	116493713
10	10779804	10779805	G	A	19	GENIC	homozygous	116493715
10	10780292	10780294	CT		20	GENIC	homozygous	128789529
10	10780307	10780309	AT		19	GENIC	homozygous	128789530
10	10780382	10780383	G	A	33	GENIC	homozygous	116493717
10	10780412	10780413	T	A	37	GENIC	homozygous	116493719
10	10780413	10780414	C	A	37	GENIC	homozygous	116493721
10	10782736	10782737	T	C	32	GENIC	homozygous	116493723
10	10782804	10782805	G	A	23	GENIC	homozygous	116493725
10	10779706	10779707	C	T	18	GENIC	homozygous	117102508
10	10779719	10779720	C	T	16	GENIC	homozygous	117140125
10	10780296	10780297	C	T	20	GENIC	homozygous	117119890
10	10783067	10783068	G	T	20	GENIC	homozygous	116734080
10	10784266	10784267	G	A	24	GENIC	homozygous	116734081