chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	10176574	10176575	T	C	42	GENIC	homozygous	138001086
7	10176601	10176602	C	T	48	GENIC	homozygous	138001087
7	10177439	10177441	TT		21	GENIC	homozygous	137934968
7	10177749	10177750	C	A	19	GENIC	homozygous	138001088
7	10180248	10180249	C	T	28	GENIC	homozygous	138001089
7	10180254	10180255	C	T	28	GENIC	homozygous	138001090
7	10181168	10181169	A	G	35	GENIC	homozygous	138001091
7	10181294	10181295	A	G	44	GENIC	homozygous	138001092
7	10181605	10181606	G	A	41	GENIC	homozygous	138001093
7	10182033	10182034	G		8	GENIC	heterozygous	403199769
7	10180230	10180231	C	T	47	GENIC	homozygous	154428496
7	10180230	10180231	C		47	GENIC	heterozygous	403199765
7	10182032	10182033	A	G	8	GENIC	heterozygous	403199766
7	10182032	10182033	A		8	GENIC	heterozygous	403199767
7	10182033	10182034	G	C	8	GENIC	heterozygous	403199768
7	10182034	10182035	A	G	8	GENIC	heterozygous	403199770
7	10182034	10182035	A		8	GENIC	heterozygous	403199771
7	10182042	10182043	A	G	8	GENIC	heterozygous	404076817
7	10182042	10182043	A		8	GENIC	heterozygous	404076818
7	10182083	10182084	G	C	8	GENIC	heterozygous	154428498
7	10182083	10182084	G		8	GENIC	heterozygous	404399131
7	10182087	10182088	G	C	9	GENIC	heterozygous	154428499
7	10182777	10182778	T	C	59	GENIC	homozygous	138001096
7	10183595	10183596	G	A	40	GENIC	homozygous	138001097
7	10182242	10182242		AC	21	GENIC	possibly homozygous	140891664