chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66133377	66133378	C	-	12	GENIC	homozygous	51907758
10	66134607	66134608	T	-	4	GENIC	heterozygous	52440880
10	66134758	66134759	C	CTCTG	11	GENIC	homozygous	51479126
10	66134759	66134760	A	G	11	GENIC	homozygous	52382562
10	66137130	66137131	T	-	2	GENIC	homozygous	52382566
10	66140930	66140931	C	G	9	GENIC	homozygous	51479147
10	66140931	66140932	C	A	9	GENIC	homozygous	51479148
10	66140939	66140940	G	T	9	GENIC	homozygous	51479149
10	66140941	66140942	A	-	9	GENIC	homozygous	51479150
10	66140944	66140945	T	C	9	GENIC	homozygous	52382568
10	66140945	66140946	A	T	9	GENIC	homozygous	52382570
10	66140958	66140959	G	C	10	GENIC	homozygous	51479151
10	66140960	66140961	G	T	10	GENIC	homozygous	51479152
10	66140963	66140964	G	T	10	GENIC	homozygous	51479153
10	66140966	66140967	T	-	11	GENIC	homozygous	51479154
10	66140985	66140986	A	T	12	GENIC	homozygous	51479155
10	66140987	66140988	G	A	12	GENIC	homozygous	51479156
10	66140990	66140991	A	-	12	GENIC	homozygous	51479157
10	66141000	66141001	A	-	9	GENIC	homozygous	51479158
10	66141014	66141015	A	-	8	GENIC	homozygous	51479159
10	66141028	66141029	A	-	5	GENIC	homozygous	51479160
10	66141052	66141054	TG	--	1	GENIC	homozygous	51479164
10	66141089	66141090	A	-	1	GENIC	homozygous	51479168
10	66141109	66141110	C	CA	3	GENIC	homozygous	51479169
10	66141192	66141199	CCCAGCC	-------	10	GENIC	homozygous	51479170
10	66141506	66141507	G	GAA	11	GENIC	heterozygous	51479171
10	66141506	66141507	G	GA	11	GENIC	heterozygous	51678674
10	66143991	66143995	TTTT	----	4	GENIC	heterozygous	51479172
10	66143994	66143995	T	-	4	GENIC	heterozygous	52320363
10	66147013	66147014	A	-	6	GENIC	heterozygous	51479180
10	66147045	66147046	G	-	8	GENIC	homozygous	51479181
10	66156768	66156769	A	G	18	GENIC	homozygous	51479193
10	66162694	66162695	A	-	5	GENIC	heterozygous	51678676