chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	85356353	85356354	A	T	34	GENIC	homozygous	116846443
8	85356576	85356577	C	T	37	GENIC	homozygous	116543432
8	85356592	85356593	C	T	34	GENIC	homozygous	117165185
8	85356616	85356617	C	T	34	GENIC	homozygous	117165187
8	85356778	85356779	A	G	52	GENIC	homozygous	116543434
8	85356793	85356794	G	T	51	GENIC	possibly homozygous	117165189
8	85356878	85356879	G	A	61	GENIC	homozygous	117165191
8	85357027	85357028	G	C	52	GENIC	homozygous	117165193
8	85357077	85357078	A	G	54	GENIC	homozygous	116543438
8	85357241	85357242	C	G	28	GENIC	homozygous	117165195
8	85357281	85357282	A	G	22	GENIC	homozygous	116543440
8	85357298	85357299	G	C	18	GENIC	homozygous	116543442
8	85357795	85357796	A	C	44	GENIC	homozygous	117165197
8	85357825	85357826	A	G	47	GENIC	homozygous	117165199
8	85358039	85358040	G	A	57	GENIC	possibly homozygous	117165201
8	85359142	85359143	A	G	26	GENIC	homozygous	116543450
8	85359484	85359485	G	A	52	GENIC	homozygous	116543452
8	85360292	85360293	A	G	50	GENIC	homozygous	117165203
8	85361467	85361468	G	A	47	GENIC	homozygous	117165205
8	85362192	85362193	C	A	66	GENIC	homozygous	117165207
8	85363775	85363776	G	T	49	GENIC	possibly homozygous	117165209
8	85364026	85364027	C	T	42	GENIC	homozygous	117165211
8	85368251	85368252	A	G	56	GENIC	homozygous	116543488