chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95922915	95922916	G	A	31	GENIC	homozygous	117022617
10	95923129	95923130	C	T	19	GENIC	homozygous	116907011
10	95924592	95924593	A	G	37	GENIC	homozygous	116688492
10	95926476	95926477	G	A	23	GENIC	homozygous	116688498
10	95926681	95926682	G	A	18	GENIC	homozygous	117022618
10	95926697	95926698	G	C	21	GENIC	homozygous	116688500
10	95927445	95927446	C	G	15	GENIC	homozygous	117022619
10	95928070	95928071	A	G	35	GENIC	homozygous	116688506
10	95928103	95928104	T	C	18	GENIC	homozygous	116688508
10	95931227	95931228	A	G	25	GENIC	homozygous	117022620
10	95931350	95931351	C	T	33	GENIC	homozygous	116688532
10	95931514	95931515	A	C	23	GENIC	homozygous	116688534
10	95931645	95931646	C	G	25	GENIC	homozygous	116688536
10	95932299	95932300	A	G	24	GENIC	homozygous	116688544
10	95932311	95932312	G	C	18	GENIC	homozygous	117022621
10	95932411	95932412	T	C	21	GENIC	homozygous	117022622
10	95932457	95932458	G	A	26	GENIC	homozygous	117022623
10	95932582	95932583	C	G	28	GENIC	homozygous	117022624
10	95932616	95932617	C	T	26	GENIC	homozygous	117022625
10	95932617	95932618	G	A	25	GENIC	homozygous	117022626
10	95932624	95932625	A	T	21	GENIC	homozygous	117022627
10	95932762	95932763	A	G	28	GENIC	homozygous	117022628
10	95933432	95933433	C	A	34	GENIC	homozygous	116688550
10	95934131	95934132	G	T	20	GENIC	homozygous	117022629