chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	132064535	132064536	A	C	24	GENIC	homozygous	52900602
8	132065295	132065296	T	G	31	GENIC	homozygous	52900603
8	132073707	132073708	G	A	53	GENIC	homozygous	52900605
8	132076186	132076187	A	T	26	GENIC	homozygous	52900607
8	132077007	132077008	T	C	40	GENIC	homozygous	52900609
8	132078522	132078523	A	T	54	GENIC	homozygous	52900611
8	132081306	132081307	G	GT	24	GENIC	heterozygous	52900613
8	132082064	132082065	G	T	33	GENIC	homozygous	52900615
8	132082755	132082756	C	T	32	GENIC	homozygous	52900617
8	132083018	132083019	C	CATCT	15	GENIC	heterozygous	52900619
8	132083019	132083031	ATCTATCTATCT	------------	15	GENIC	possibly homozygous	52900621
8	132083514	132083515	G	A	32	GENIC	homozygous	52900623
8	132083882	132083883	G	C	18	GENIC	homozygous	52900625
8	132083961	132083962	A	-	14	GENIC	homozygous	52900627
8	132084082	132084083	C	A	14	GENIC	homozygous	52900629
8	132084980	132084981	G	A	18	GENIC	homozygous	52900631
8	132086091	132086092	G	A	24	GENIC	homozygous	52900633
8	132089079	132089080	C	T	42	GENIC	homozygous	52900635
8	132089095	132089096	T	C	47	GENIC	homozygous	52900637
8	132089321	132089322	A	G	38	GENIC	homozygous	52900639
8	132090262	132090263	T	TTG	1	GENIC	homozygous	52900641