chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	132699382	132699383	G	A	42	GENIC	homozygous	141250070
1	132699616	132699617	C	T	43	GENIC	homozygous	141250071
1	132700051	132700070	GCTCAACATGTGAAAGAAA		41	GENIC	homozygous	141169197
1	132700461	132700462	T	C	16	GENIC	possibly homozygous	144556199
1	132700522	132700523	C	G	15	GENIC	homozygous	144556200
1	132701268	132701269	A	T	51	GENIC	homozygous	135670175
1	132702264	132702265	A	G	39	GENIC	homozygous	141250072
1	132702403	132702404	C	T	52	GENIC	homozygous	141250073
1	132702517	132702518	G	A	44	GENIC	homozygous	135670178
1	132703266	132703267	G	A	56	GENIC	homozygous	141250074
1	132703563	132703564	G	A	45	GENIC	homozygous	141250075
1	132700464	132700470	CAGTCC		16	GENIC	possibly homozygous	144525751
1	132704524	132704525	C		16	GENIC	possibly homozygous	144525752
1	132704524	132704525	C	G	16	GENIC	heterozygous	402963799
1	132704524	132704525	C	A	16	GENIC	heterozygous	402963800
1	132700491	132700492	A		15	GENIC	heterozygous	402963797
1	132700491	132700492	A	T	15	GENIC	homozygous	402963798
1	132704532	132704533	C	A	16	GENIC	possibly homozygous	402963801
1	132704532	132704533	C		16	GENIC	heterozygous	402963802
1	132704544	132704545	A	C	16	GENIC	possibly homozygous	153803109
1	132704544	132704545	A		16	GENIC	heterozygous	402963803
1	132705062	132705063	G	A	51	GENIC	homozygous	141250076
1	132705351	132705352	G	A	47	GENIC	homozygous	141250077
1	132706242	132706243	T	C	46	GENIC	homozygous	135670188
1	132706995	132706996	A	G	42	GENIC	homozygous	135670189
1	132707299	132707300	C	G	44	GENIC	homozygous	141250078