chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	132181201	132181202	G	C	21	GENIC	homozygous	53066987
8	132182342	132182343	G	A	26	GENIC	homozygous	53066988
8	132182399	132182400	T	-	14	GENIC	homozygous	53066989
8	132183388	132183389	G	C	32	GENIC	homozygous	53066990
8	132183543	132183544	G	GA	29	GENIC	possibly homozygous	53306673
8	132183918	132183919	T	A	16	GENIC	homozygous	53066991
8	132184063	132184064	C	T	17	GENIC	homozygous	53066992
8	132185741	132185742	C	T	26	GENIC	homozygous	53066993
8	132185858	132185859	T	TA	18	GENIC	possibly homozygous	53183998
8	132186226	132186227	T	C	22	GENIC	homozygous	53066994
8	132186716	132186717	T	C	27	GENIC	homozygous	52900835
8	132187360	132187361	G	T	23	GENIC	homozygous	53066995
8	132187646	132187647	T	TA	11	GENIC	homozygous	53066996
8	132188191	132188192	T	C	21	GENIC	homozygous	53066997
8	132188489	132188507	TAATAATAATAATAATAA	------------------	9	GENIC	homozygous	53456342
8	132189090	132189091	C	T	20	GENIC	homozygous	52900837
8	132190590	132190591	A	G	24	GENIC	homozygous	53066999
8	132190602	132190603	A	G	18	GENIC	homozygous	53067000