chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110148567	110148568	A	G	60	GENIC	homozygous	116719525
10	110152178	110152179	T	C	27	GENIC	homozygous	116719531
10	110152648	110152649	T	C	62	GENIC	homozygous	116909934
10	110156732	110156733	G	A	54	GENIC	homozygous	118054358
10	110157027	110157028	C	T	43	GENIC	possibly homozygous	116719533
10	110160865	110160866	A	G	44	GENIC	homozygous	116719537
10	110162051	110162052	C	T	51	GENIC	homozygous	116719541
10	110163475	110163476	A	G	46	GENIC	possibly homozygous	118013252
10	110165233	110165234	T	C	24	GENIC	possibly homozygous	118054359
10	110165245	110165246	T	C	18	GENIC	homozygous	118054360
10	110165252	110165253	T	C	13	GENIC	homozygous	118054361
10	110166113	110166114	C	T	11	GENIC	possibly homozygous	118054362
10	110166123	110166124	A	G	14	GENIC	possibly homozygous	118054363
10	110166129	110166130	C	A	20	GENIC	possibly homozygous	118054364
10	110166134	110166135	C	G	22	GENIC	possibly homozygous	118054365
10	110166140	110166141	T	C	27	GENIC	possibly homozygous	118054366
10	110170589	110170590	A	G	44	GENIC	heterozygous	118013253
10	110171579	110171580	C	T	91	GENIC	homozygous	118054367
10	110172213	110172214	G	A	62	GENIC	homozygous	118054368
10	110173599	110173600	C	T	61	GENIC	heterozygous	118013254
10	110173907	110173908	A	G	57	GENIC	homozygous	118054369
10	110174617	110174618	G	A	40	GENIC	homozygous	116719561
10	110177510	110177511	T	C	53	GENIC	possibly homozygous	118054370
10	110177786	110177787	A	G	66	GENIC	homozygous	116719565
10	110180154	110180155	G	T	60	GENIC	homozygous	118054371