chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	83921996	83921997	T	G	30	GENIC	homozygous	116662389
10	83922023	83922024	T	G	28	GENIC	homozygous	116662391
10	83923258	83923259	T	C	27	GENIC	homozygous	117018366
10	83923348	83923349	G	C	16	GENIC	homozygous	116813757
10	83923931	83923932	A	G	29	GENIC	homozygous	116662401
10	83925935	83925936	A	C	34	GENIC	homozygous	117018367
10	83925988	83925989	C	T	24	GENIC	homozygous	116813773
10	83926165	83926166	T	G	25	GENIC	homozygous	116662407
10	83926516	83926517	A	T	33	GENIC	homozygous	117018368
10	83926898	83926899	A	C	14	GENIC	homozygous	117018369
10	83927018	83927019	C	T	27	GENIC	homozygous	117018370
10	83927223	83927224	G	A	26	GENIC	homozygous	116662421
10	83927322	83927323	T	C	24	GENIC	homozygous	116662423
10	83927324	83927325	T	C	24	GENIC	homozygous	116662425
10	83927326	83927327	T	G	22	GENIC	homozygous	116662427
10	83928518	83928519	A	C	23	GENIC	homozygous	116662429
10	83928520	83928521	G	A	22	GENIC	homozygous	116662431
10	83928630	83928631	T	C	28	GENIC	homozygous	117018371
10	83928960	83928961	C	G	25	GENIC	homozygous	116662433
10	83931148	83931149	T	C	25	GENIC	homozygous	116662435
10	83931675	83931676	G	A	38	GENIC	homozygous	117018372
10	83932375	83932376	T	C	29	GENIC	homozygous	117018373
10	83932642	83932643	G	A	27	GENIC	homozygous	117018374