chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	49201203	49201204	T	A	24	GENIC	homozygous	116881861
10	49201362	49201363	A	G	23	GENIC	homozygous	116881863
10	49201730	49201731	C	G	19	GENIC	homozygous	116881865
10	49201834	49201835	C	T	24	GENIC	homozygous	116881867
10	49201950	49201951	C	G	21	GENIC	homozygous	116881869
10	49202001	49202002	A	G	16	GENIC	homozygous	117129669
10	49202133	49202134	G	A	17	GENIC	homozygous	117129671
10	49202207	49202208	G	A	30	GENIC	homozygous	117129673
10	49202503	49202504	T	C	19	GENIC	homozygous	116881871
10	49202529	49202530	C	T	26	GENIC	homozygous	117129675
10	49203223	49203224	T	A	18	GENIC	homozygous	116881875
10	49203496	49203497	T	C	19	GENIC	homozygous	116881877
10	49204487	49204488	T	C	12	GENIC	homozygous	116881881
10	49204805	49204806	A	G	13	GENIC	homozygous	116881885
10	49205037	49205038	C	T	27	GENIC	homozygous	116881887
10	49205906	49205907	G	C	36	GENIC	homozygous	116881891
10	49205914	49205915	T	C	35	GENIC	homozygous	116881893
10	49206720	49206721	C	T	22	GENIC	homozygous	116881895
10	49206882	49206883	A	T	18	GENIC	homozygous	116881897
10	49207317	49207318	A	G	28	GENIC	homozygous	117103866
10	49207462	49207463	C	T	22	GENIC	homozygous	116881901
10	49207492	49207493	C	T	26	GENIC	possibly homozygous	116881903
10	49209280	49209281	C	T	19	GENIC	homozygous	116881905
10	49209299	49209300	C	T	18	GENIC	homozygous	116881907
10	49209731	49209732	C	T	25	GENIC	possibly homozygous	116881909