chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	102136315	102136316	C	CGG	6	GENIC	heterozygous	52075272
10	102136568	102136569	T	G	34	GENIC	homozygous	52075274
10	102137007	102137008	T	C	34	GENIC	homozygous	51587354
10	102137857	102137858	T	C	31	GENIC	homozygous	51587360
10	102137865	102137866	A	G	32	GENIC	possibly homozygous	51587362
10	102139449	102139450	T	C	27	GENIC	homozygous	51587368
10	102139657	102139660	TTT	---	24	GENIC	homozygous	51587372
10	102139666	102139669	TTC	---	29	GENIC	heterozygous	51587374
10	102139670	102139671	T	-	26	GENIC	homozygous	52075276
10	102140144	102140145	G	C	21	GENIC	heterozygous	51760641
10	102140146	102140147	G	C	21	GENIC	heterozygous	52075278
10	102140148	102140149	G	C	21	GENIC	heterozygous	52075280
10	102140505	102140506	T	C	35	GENIC	homozygous	51587380
10	102142612	102142613	G	A	42	GENIC	homozygous	52075282
10	102143189	102143190	C	CAAAA	5	GENIC	heterozygous	51587394
10	102143189	102143190	C	CAAA	5	GENIC	heterozygous	51587396