chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	43632010	43632011	C	T	9	GENIC	homozygous	116578971
10	43632934	43632935	C	T	39	GENIC	homozygous	116578973
10	43633030	43633031	G	A	25	GENIC	homozygous	116578975
10	43634452	43634453	T	G	14	GENIC	homozygous	116578977
10	43635023	43635024	C	A	16	GENIC	homozygous	116578979
10	43635145	43635146	A	G	29	GENIC	homozygous	116578981
10	43635206	43635207	A	G	24	GENIC	homozygous	116578983
10	43635275	43635276	G	A	27	GENIC	homozygous	116578985
10	43635366	43635367	C	T	25	GENIC	homozygous	116578987
10	43635449	43635450	G	T	23	GENIC	homozygous	116578989
10	43635538	43635539	C	T	19	GENIC	homozygous	116578991
10	43635562	43635563	C	T	28	GENIC	homozygous	116578993
10	43635570	43635571	G	C	31	GENIC	homozygous	116578995
10	43635595	43635596	A	T	29	GENIC	homozygous	116578997
10	43635751	43635752	G	A	23	GENIC	homozygous	116578999
10	43635954	43635955	A	G	7	GENIC	homozygous	116579005
10	43636087	43636088	C	A	14	GENIC	homozygous	116579007
10	43636164	43636165	C	G	18	GENIC	homozygous	116579009
10	43636201	43636202	A	T	23	GENIC	homozygous	116579011
10	43636255	43636256	G	A	20	GENIC	homozygous	116579013
10	43636813	43636814	A	G	24	GENIC	homozygous	116579017
10	43636966	43636967	T	C	24	GENIC	homozygous	116579019
10	43637025	43637026	C	T	29	GENIC	homozygous	116579021
10	43637056	43637057	G	A	22	GENIC	homozygous	116579023
10	43637233	43637234	C	T	15	GENIC	possibly homozygous	116579025
10	43637299	43637300	C	T	27	GENIC	possibly homozygous	116579029
10	43637398	43637399	A	G	12	GENIC	homozygous	117277816
10	43637410	43637411	G	A	6	GENIC	homozygous	117277818
10	43638019	43638020	G	A	26	GENIC	homozygous	116579031
10	43638331	43638332	A	G	36	GENIC	homozygous	116579033
10	43638423	43638424	C	G	12	GENIC	homozygous	116579035
10	43638690	43638691	T	C	17	GENIC	homozygous	116579037
10	43638779	43638780	C	T	32	GENIC	homozygous	116579039