chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59752430	59752431	G	A	22	GENIC	homozygous	116788941
10	59755287	59755288	G	A	41	GENIC	homozygous	116788943
10	59755896	59755897	T	A	49	GENIC	homozygous	116608677
10	59756618	59756619	G	T	36	GENIC	homozygous	116788947
10	59758127	59758128	G	A	31	GENIC	homozygous	117011730
10	59758282	59758283	C	G	26	GENIC	homozygous	116788949
10	59758304	59758305	G	A	30	GENIC	homozygous	116788951
10	59758702	59758703	G	A	32	GENIC	homozygous	116608681
10	59758947	59758948	A	G	22	GENIC	homozygous	116608685
10	59760011	59760012	G	A	41	GENIC	homozygous	116788952
10	59760058	59760059	G	A	33	GENIC	homozygous	116608687
10	59760118	59760119	T	C	29	GENIC	homozygous	116788953
10	59760146	59760147	T	C	37	GENIC	homozygous	116788954
10	59760650	59760651	G	C	29	GENIC	homozygous	116608693
10	59762255	59762256	A	G	34	GENIC	homozygous	116788956
10	59763411	59763412	T	C	29	GENIC	homozygous	116608699
10	59763614	59763615	A	G	28	GENIC	homozygous	116788957
10	59763711	59763712	G	A	29	GENIC	homozygous	116937880
10	59763717	59763718	C	T	33	GENIC	homozygous	116788958
10	59763726	59763727	G	A	35	GENIC	homozygous	116788959
10	59763755	59763756	C	T	37	GENIC	homozygous	116788960
10	59764194	59764195	T	G	28	GENIC	homozygous	116788961
10	59764810	59764811	T	C	25	GENIC	homozygous	116788962
10	59765814	59765815	A	G	29	GENIC	homozygous	116788963
10	59765908	59765909	C	T	28	GENIC	homozygous	116788964
10	59766366	59766367	A	G	42	GENIC	homozygous	116788965
10	59768072	59768073	A	G	25	GENIC	homozygous	116788966
10	59768734	59768735	T	G	38	GENIC	homozygous	116788967
10	59768761	59768762	T	C	45	GENIC	homozygous	116788968
10	59769766	59769767	C	T	35	GENIC	homozygous	116788969
10	59770639	59770640	C	A	34	GENIC	homozygous	116608703
10	59770640	59770641	T	G	35	GENIC	homozygous	116788970
10	59770745	59770746	T	C	32	GENIC	homozygous	116788971
10	59770990	59770991	A	G	32	GENIC	homozygous	116788972
10	59771209	59771210	A	G	36	GENIC	homozygous	116788973