chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	48626499	48626500	G	A	50	GENIC	homozygous	117002503
8	48626614	48626615	A	T	55	GENIC	homozygous	117002505
8	48626697	48626698	G	A	78	GENIC	possibly homozygous	117002507
8	48627857	48627858	T	C	42	GENIC	homozygous	118096757
8	48629377	48629378	T	A	47	GENIC	homozygous	118096759
8	48629748	48629749	G	A	64	GENIC	homozygous	117002515
8	48631596	48631600	TCTG		69	GENIC	homozygous	133559770
8	48631960	48631961	G	A	55	GENIC	homozygous	118096761
8	48632030	48632031	T	C	60	GENIC	homozygous	117002517
8	48632548	48632549	T	C	58	GENIC	possibly homozygous	118096763
8	48632781	48632782	G	A	57	GENIC	homozygous	116957250
8	48632874	48632875	C	T	52	GENIC	homozygous	117002521
8	48633554	48633555	C	A	42	GENIC	homozygous	116957252
8	48634362	48634363	A	G	31	GENIC	homozygous	116957254
8	48634367	48634368	A	T	30	GENIC	homozygous	118096764
8	48634423	48634432	AGGGGAAGG		27	GENIC	homozygous	133559771
8	48634446	48634449	GAA		22	GENIC	homozygous	133559772
8	48634483	48634485	AT		22	GENIC	homozygous	133559773
8	48634716	48634717	T	C	39	GENIC	homozygous	116957258
8	48634866	48634867	A	G	51	GENIC	homozygous	116957260
8	48635614	48635615	T	A	59	GENIC	homozygous	118096766
8	48635688	48635689	T	C	56	GENIC	homozygous	116957262
8	48635824	48635827	TCC		40	GENIC	homozygous	132122116
8	48636227	48636228	C	G	54	GENIC	homozygous	117002523
8	48636483	48636484	G	A	20	GENIC	homozygous	118096768
8	48636637	48636638	C	T	18	GENIC	homozygous	133561584
8	48637048	48637048		ACG	38	GENIC	homozygous	133559774