chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110560098	110560099	T	C	47	GENIC	homozygous	116720872
10	110560622	110560623	A	G	47	GENIC	homozygous	116720874
10	110562172	110562173	G	A	39	GENIC	homozygous	116720876
10	110562498	110562499	C	A	35	GENIC	homozygous	116720878
10	110562668	110562669	A	C	45	GENIC	homozygous	116720880
10	110563469	110563470	T	C	46	GENIC	homozygous	116720882
10	110564557	110564558	C	T	49	GENIC	homozygous	116720884
10	110564609	110564610	T	A	65	GENIC	homozygous	116720886
10	110564749	110564750	G	A	67	GENIC	homozygous	116720888
10	110564843	110564844	G	A	66	GENIC	homozygous	116720890
10	110564903	110564904	A	G	56	GENIC	homozygous	116720892
10	110565217	110565218	T	A	53	GENIC	homozygous	116720894
10	110565533	110565534	A	G	43	GENIC	homozygous	116720896
10	110565715	110565716	C	T	43	GENIC	homozygous	116720898
10	110568837	110568838	G	A	41	GENIC	homozygous	116720900
10	110570228	110570229	G	A	23	GENIC	homozygous	116720904
10	110571010	110571011	A	T	53	GENIC	homozygous	116720906
10	110574509	110574510	T	C	49	GENIC	possibly homozygous	116720908
10	110576055	110576056	C	T	48	GENIC	possibly homozygous	116720910
10	110576265	110576266	T	C	54	GENIC	homozygous	116720912
10	110577347	110577348	C	T	42	GENIC	homozygous	116720914
10	110577575	110577576	G	A	50	GENIC	homozygous	116720916
10	110578753	110578754	G	A	41	GENIC	homozygous	116720918
10	110579985	110579986	A	G	42	GENIC	homozygous	116720920
10	110580369	110580370	A	G	47	GENIC	homozygous	116720922
10	110580404	110580405	A	G	45	GENIC	homozygous	116720924
10	110580510	110580511	T	G	40	GENIC	homozygous	116720926
10	110580836	110580837	C	T	18	GENIC	homozygous	116720930
10	110582071	110582072	T	C	51	GENIC	homozygous	116720932
10	110585157	110585158	T	C	40	GENIC	homozygous	116720934