chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	132135782	132135783	G	A	22	INTERGENIC	homozygous	53066893
8	132136237	132136238	A	G	21	INTERGENIC	possibly homozygous	53066894
8	132136461	132136462	A	G	26	INTERGENIC	homozygous	53066895
8	132136527	132136528	C	T	18	INTERGENIC	possibly homozygous	53066896
8	132136675	132136676	C	T	22	INTERGENIC	homozygous	53066897
8	132137102	132137103	A	C	20	INTERGENIC	possibly homozygous	53066898
8	132140793	132140794	G	A	14	INTERGENIC	homozygous	53066899
8	132141058	132141059	G	GTT	3	INTERGENIC	homozygous	53066900
8	132141848	132141849	T	G	18	INTERGENIC	homozygous	53066901
8	132142952	132142953	G	GT	8	INTERGENIC	heterozygous	53066902
8	132149316	132149317	G	A	30	GENIC	possibly homozygous	52900704
8	132149392	132149393	G	T	22	GENIC	possibly homozygous	52900706
8	132150509	132150510	T	TATC	1	GENIC	homozygous	52900710
8	132152331	132152332	C	T	15	GENIC	homozygous	53066907
8	132152697	132152698	T	-	15	GENIC	homozygous	52900716
8	132152793	132152794	A	G	13	GENIC	homozygous	53066908
8	132152988	132152989	G	A	7	GENIC	homozygous	52900717
8	132153662	132153663	A	G	21	INTERGENIC	possibly homozygous	52900719
8	132154590	132154594	GAAA	----	6	INTERGENIC	heterozygous	52900723
8	132155334	132155335	A	C	7	INTERGENIC	possibly homozygous	52900735
8	132156121	132156122	G	A	6	INTERGENIC	heterozygous	53066912
8	132156149	132156150	T	C	13	INTERGENIC	possibly homozygous	52900757
8	132156166	132156167	C	T	14	INTERGENIC	possibly homozygous	53066913
8	132156345	132156346	G	A	16	INTERGENIC	possibly homozygous	52900761
8	132156372	132156373	C	T	12	INTERGENIC	homozygous	53066914