chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	59510440	59510441	T	C	54	GENIC	homozygous	140331102
18	59511403	59511404	A	G	55	GENIC	homozygous	140331103
18	59511584	59511585	C	T	49	GENIC	homozygous	140331104
18	59512175	59512175		TA	55	GENIC	homozygous	140226848
18	59512761	59512762	T	C	51	GENIC	homozygous	140331105
18	59513445	59513446	T	A	41	GENIC	homozygous	140331106
18	59513731	59513732	C	G	66	GENIC	homozygous	140331107
18	59514741	59514742	A	G	42	GENIC	homozygous	140331108
18	59516180	59516181	A	T	44	GENIC	homozygous	140331109
18	59516917	59516918	G	C	53	GENIC	homozygous	140331110
18	59517951	59517952	T	A	51	GENIC	homozygous	140331111
18	59519831	59519831		T	64	GENIC	homozygous	140226849
18	59519833	59519839	CCCCAC		65	GENIC	homozygous	140226850
18	59519842	59519843	T	G	63	GENIC	homozygous	140331112
18	59519844	59519845	C	G	61	GENIC	homozygous	140331113
18	59519850	59519851	T		61	GENIC	homozygous	140226851
18	59519851	59519852	T	A	62	GENIC	homozygous	140331114
18	59520750	59520759	GTAATTCCA		45	GENIC	possibly homozygous	140226852
18	59521072	59521083	ATGAGGCAGAC		45	GENIC	homozygous	140226853
18	59520750	59520751	G		45	GENIC	possibly homozygous	403436585
18	59514650	59514651	C	A	35	GENIC	heterozygous	155096475
18	59520750	59520751	G	T	45	GENIC	heterozygous	155097548
18	59514650	59514651	C		35	GENIC	homozygous	403436584
18	59523846	59523847	T	C	58	GENIC	possibly homozygous	140331115
18	59523894	59523895	T	A	62	GENIC	homozygous	140331116
18	59524274	59524275	G	A	50	GENIC	homozygous	140331117
18	59524348	59524348		G	46	GENIC	homozygous	140226854
18	59524864	59524865	A	C	28	GENIC	homozygous	140331118
18	59528491	59528492	G	A	49	GENIC	homozygous	140331119