chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	46296079	46296080	C	G	37	GENIC	homozygous	53318270
8	46296666	46296667	T	C	32	GENIC	homozygous	53106977
8	46296755	46296756	A	T	38	GENIC	homozygous	53318271
8	46296770	46296771	T	C	32	GENIC	homozygous	53318272
8	46296771	46296772	T	G	32	GENIC	homozygous	53318273
8	46296847	46296848	T	TGTATGGGCCTAA	21	GENIC	homozygous	53318274
8	46296876	46296877	A	T	24	GENIC	homozygous	53318275
8	46296896	46296897	A	G	26	GENIC	homozygous	53318276
8	46297029	46297030	T	C	31	GENIC	homozygous	53318277
8	46297030	46297031	G	A	31	GENIC	homozygous	53318278
8	46297703	46297704	G	A	28	GENIC	homozygous	53318279
8	46302015	46302016	T	G	30	GENIC	homozygous	53106982
8	46302103	46302104	G	T	25	GENIC	homozygous	53318280
8	46304151	46304152	T	-	29	GENIC	homozygous	53318281
8	46304851	46304853	TT	--	20	GENIC	homozygous	53181484
8	46305435	46305439	CATC	----	27	GENIC	homozygous	52619795
8	46309055	46309056	G	A	40	GENIC	homozygous	53106997
8	46309804	46309805	A	G	37	GENIC	homozygous	53107000
8	46310957	46310958	C	T	19	GENIC	homozygous	53107001
8	46311112	46311113	C	T	31	GENIC	homozygous	53107002
8	46311624	46311625	T	G	39	GENIC	homozygous	53107003
8	46313104	46313105	A	G	33	GENIC	homozygous	53107006
8	46315264	46315265	C	G	30	GENIC	homozygous	53318282
8	46318474	46318475	A	G	26	GENIC	homozygous	53107013