chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	10176574	10176575	T	C	65	GENIC	homozygous	138001086
7	10176601	10176602	C	T	67	GENIC	homozygous	138001087
7	10177439	10177441	TT		16	GENIC	heterozygous	137934968
7	10177749	10177750	C	A	20	GENIC	homozygous	138001088
7	10180248	10180249	C	T	30	GENIC	homozygous	138001089
7	10180254	10180255	C	T	30	GENIC	homozygous	138001090
7	10181168	10181169	A	G	41	GENIC	homozygous	138001091
7	10181294	10181295	A	G	43	GENIC	homozygous	138001092
7	10181605	10181606	G	A	41	GENIC	homozygous	138001093
7	10180230	10180231	C		45	GENIC	heterozygous	403199765
7	10180230	10180231	C	T	45	GENIC	homozygous	154428496
7	10182315	10182316	G	C	22	GENIC	homozygous	138001094
7	10182328	10182330	AG		22	GENIC	homozygous	137934969
7	10182364	10182366	AC		5	GENIC	heterozygous	137934970
7	10182403	10182404	G	C	8	GENIC	possibly homozygous	403199772
7	10182403	10182404	G		8	GENIC	heterozygous	403199773
7	10182405	10182406	G	C	8	GENIC	possibly homozygous	403199774
7	10182405	10182406	G		8	GENIC	heterozygous	403199775
7	10182407	10182408	G	C	8	GENIC	possibly homozygous	138001095
7	10182777	10182778	T	C	59	GENIC	homozygous	138001096
7	10183595	10183596	G	A	56	GENIC	homozygous	138001097
7	10182387	10182388	G	C	5	GENIC	heterozygous	146827460
7	10182242	10182242		AC	11	GENIC	possibly homozygous	140891664
7	10182384	10182384		AC	5	GENIC	heterozygous	146817026