chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94506652	94506653	T	C	22	GENIC	heterozygous	53166837
10	94506658	94506659	G	A	20	GENIC	heterozygous	53166839
10	94506673	94506674	G	C	20	GENIC	heterozygous	53166841
10	94506737	94506738	A	C	15	GENIC	heterozygous	53166843
10	94506739	94506740	T	C	15	GENIC	heterozygous	53166845
10	94506885	94506886	G	A	15	GENIC	heterozygous	53166847
10	94506945	94506946	A	G	8	GENIC	heterozygous	51549038
10	94507023	94507024	A	G	14	GENIC	heterozygous	53166849
10	94507026	94507027	A	G	15	GENIC	heterozygous	53166851
10	94507656	94507657	C	T	18	GENIC	heterozygous	53166853
10	94507964	94507965	C	T	19	GENIC	heterozygous	53166855
10	94508016	94508017	T	G	18	GENIC	heterozygous	51549040
10	94508598	94508599	T	C	19	GENIC	heterozygous	53166857
10	94537337	94537338	A	G	22	GENIC	heterozygous	51549150
10	94537389	94537390	C	G	19	GENIC	heterozygous	53167225
10	94537404	94537405	T	C	19	GENIC	heterozygous	53167227
10	94538340	94538341	A	G	49	GENIC	heterozygous	53167263
10	94538444	94538445	C	A	15	GENIC	heterozygous	53167265
10	94541586	94541587	T	C	42	GENIC	heterozygous	53167315
10	94541587	94541588	G	A	41	GENIC	heterozygous	53167317
10	94551697	94551698	C	T	6	GENIC	heterozygous	53167518
10	94554783	94554784	A	G	19	GENIC	heterozygous	52996818