chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66458537	66458538	T	C	41	GENIC	homozygous	51908217
10	66459601	66459602	G	GA	28	GENIC	homozygous	51908219
10	66459832	66459833	A	-	39	GENIC	homozygous	51908221
10	66460458	66460459	C	T	25	GENIC	homozygous	51479799
10	66461046	66461047	C	CTTTT	19	GENIC	homozygous	51908223
10	66461295	66461296	G	A	16	GENIC	homozygous	51908225
10	66462098	66462099	T	-	19	GENIC	homozygous	51987873
10	66462488	66462490	TT	--	11	GENIC	possibly homozygous	51908227
10	66464544	66464545	G	-	18	GENIC	homozygous	51479801
10	66464640	66464641	C	T	13	GENIC	homozygous	51908228
10	66464758	66464759	T	TA	23	GENIC	homozygous	51479802
10	66465362	66465363	T	A	20	GENIC	homozygous	51908232
10	66465481	66465482	A	AGT	17	GENIC	homozygous	51908234
10	66466286	66466287	A	AC	2	GENIC	homozygous	51479804
10	66469026	66469027	T	TATTC	8	GENIC	homozygous	51908236
10	66469192	66469193	G	GT	15	GENIC	homozygous	51479810
10	66477792	66477793	T	TA	3	GENIC	homozygous	53027755
10	66477766	66477768	TA	--	6	GENIC	homozygous	52724645
10	66460659	66460660	C	-	31	GENIC	homozygous	51678751
10	66464797	66464798	C	CAG	21	GENIC	possibly homozygous	52382704
10	66466288	66466289	A	C	2	GENIC	homozygous	52382706
10	66462489	66462490	T	-	11	GENIC	heterozygous	52648794
10	66469301	66469302	T	A	8	GENIC	homozygous	52320389