chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	51789307	51789308	G	C	12	GENIC	heterozygous	45806223
20	51789381	51789387	CCCGCT	------	8	GENIC	heterozygous	45652074
20	51793845	51793846	C	T	119	GENIC	heterozygous	45595890
20	51793852	51793853	C	CT	153	GENIC	heterozygous	45595894
20	51814635	51814636	C	T	19	GENIC	heterozygous	45769599
20	51829269	51829270	G	T	19	GENIC	heterozygous	46121884
20	51829270	51829271	T	G	19	GENIC	heterozygous	46121886
20	51829272	51829273	A	T	19	GENIC	heterozygous	46121888
20	51829284	51829285	A	-	20	GENIC	heterozygous	45596238
20	51829303	51829304	T	A	18	GENIC	heterozygous	46121890
20	51829304	51829305	C	T	18	GENIC	heterozygous	46121892
20	51829305	51829306	G	C	18	GENIC	heterozygous	46121894
20	51840896	51840897	T	C	46	GENIC	heterozygous	45769666
20	51840962	51840963	G	A	31	GENIC	heterozygous	45769668
20	51841001	51841002	G	A	23	GENIC	heterozygous	45769670
20	51878434	51878435	T	C	14	GENIC	heterozygous	45652528
20	51878435	51878436	G	A	14	GENIC	heterozygous	45652530
20	51885105	51885106	G	A	19	GENIC	heterozygous	45652584
20	51885411	51885412	T	C	26	GENIC	heterozygous	45652588
20	51885421	51885422	T	C	25	GENIC	heterozygous	45596977
20	51885441	51885442	C	T	21	GENIC	heterozygous	45806305