chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	85668629	85668630	T	A	39	GENIC	homozygous	145747951
10	85669018	85669020	AA		30	GENIC	homozygous	145731271
10	85669533	85669533		A	29	GENIC	homozygous	145731272
10	85670843	85670844	G	T	51	GENIC	possibly homozygous	145747952
10	85671635	85671642	AGTATAT		41	GENIC	homozygous	145731273
10	85673322	85673323	G	A	41	GENIC	homozygous	145747953
10	85675502	85675502		C	48	GENIC	homozygous	138696755
10	85669672	85669673	A	G	37	GENIC	homozygous	138841598
10	85671990	85671994	TCTA		30	GENIC	homozygous	138696753
10	85672498	85672498		CAGAGCATGAATCCC	42	GENIC	homozygous	138696754
10	85675880	85675881	C	T	44	GENIC	homozygous	145747954
10	85676779	85676780	C	T	51	GENIC	homozygous	138841602
10	85676854	85676855	T	C	28	GENIC	homozygous	138841603
10	85677681	85677682	T	A	41	GENIC	homozygous	138841604
10	85678304	85678305	T	C	9	GENIC	homozygous	138841605
10	85678620	85678621	T	C	19	GENIC	possibly homozygous	145747955
10	85680632	85680632		ACAAAAAACAAAAAAC	15	GENIC	heterozygous	145731274
10	85680634	85680634		C	14	GENIC	heterozygous	145731275
10	85680845	85680846	T	C	39	GENIC	homozygous	138841606
10	85681140	85681141	A	G	43	GENIC	possibly homozygous	138841607
10	85681795	85681796	T	C	36	GENIC	homozygous	145747956
10	85682460	85682461	A	G	23	GENIC	homozygous	138841608
10	85684430	85684430		G	49	GENIC	homozygous	138696756
10	85684962	85684963	A	G	36	GENIC	homozygous	138841611
10	85686453	85686454	T	C	39	GENIC	homozygous	138841620
10	85676883	85676884	G		20	GENIC	homozygous	403293576
10	85676883	85676884	G	T	20	GENIC	heterozygous	154654769
10	85683566	85683567	G	T	46	GENIC	possibly homozygous	154654774
10	85685070	85685071	T	C	36	GENIC	homozygous	143463254
10	85685169	85685170	G	A	37	GENIC	homozygous	143463255
10	85686688	85686689	C	G	54	GENIC	homozygous	143463256