chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	108938145	108938146	C	T	55	GENIC	homozygous	114937100
6	108939410	108939411	T	C	41	GENIC	homozygous	114937101
6	108940361	108940362	T	A	33	GENIC	homozygous	114937102
6	108941830	108941831	C	T	43	GENIC	homozygous	114937103
6	108942905	108942906	A	G	74	GENIC	homozygous	114937104
6	108943608	108943611	GGA		24	GENIC	heterozygous	128380452
6	108945792	108945793	G	T	40	GENIC	homozygous	114937105
6	108946577	108946580	GGG		8	GENIC	heterozygous	128380453
6	108946580	108946581	G	T	9	GENIC	heterozygous	128422807
6	108946648	108946649	A		31	GENIC	homozygous	128380454
6	108946716	108946717	T	C	50	GENIC	homozygous	114937106
6	108946749	108946750	G	C	48	GENIC	homozygous	114937107
6	108946824	108946824		T	48	GENIC	homozygous	128380455
6	108948785	108948786	C	G	54	GENIC	homozygous	114937109
6	108950051	108950052	C	T	59	GENIC	possibly homozygous	114937110
6	108950608	108950609	T	C	64	GENIC	possibly homozygous	114937111
6	108953651	108953652	C	A	24	GENIC	possibly homozygous	114937112
6	108955758	108955759	T	A	34	GENIC	homozygous	114937113
6	108956054	108956055	A		27	GENIC	possibly homozygous	128380456
6	108957239	108957239		CC	13	GENIC	homozygous	128380457
6	108957848	108957849	G	A	46	GENIC	homozygous	114937114
6	108958953	108958954	A	G	51	GENIC	homozygous	114937115
6	108960968	108960980	GCACGCATGCAC		42	GENIC	homozygous	128380458