chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10775101	10775102	G	A	34	GENIC	homozygous	116493695
10	10775209	10775210	A	G	32	GENIC	homozygous	116913171
10	10775351	10775352	T	C	44	GENIC	homozygous	116493697
10	10776154	10776155	A	G	30	GENIC	homozygous	116493699
10	10776268	10776269	C	T	29	GENIC	homozygous	116493701
10	10776837	10776838	C	T	31	GENIC	homozygous	116493703
10	10777317	10777318	A	T	27	GENIC	homozygous	116913173
10	10778196	10778197	G	T	37	GENIC	homozygous	116493711
10	10777390	10777391	C	T	38	GENIC	homozygous	116493705
10	10778194	10778195	T	G	37	GENIC	homozygous	116493709
10	10777253	10777254	T	G	22	GENIC	homozygous	118061202
10	10778382	10778384	AC		20	GENIC	homozygous	128789527
10	10779448	10779449	A	G	47	GENIC	homozygous	116493713
10	10779706	10779707	C	T	12	GENIC	homozygous	117102508
10	10779804	10779805	G	A	23	GENIC	homozygous	116493715
10	10780177	10780178	T	G	27	GENIC	homozygous	116913175
10	10780265	10780267	AC		12	GENIC	homozygous	128789528
10	10780412	10780413	T	A	49	GENIC	homozygous	116493719
10	10780413	10780414	C	A	49	GENIC	homozygous	116493721
10	10781728	10781729	A	G	47	GENIC	homozygous	116913177
10	10782402	10782403	G	A	52	GENIC	homozygous	116913179
10	10782448	10782449	A	T	45	GENIC	homozygous	116913181
10	10784074	10784075	A	G	28	GENIC	homozygous	116493729
10	10779798	10779798		GG	19	GENIC	homozygous	132689759