chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	66350422	66350423	C	T	22	GENIC	heterozygous	52996222
10	66350423	66350424	C	T	21	GENIC	heterozygous	52996224
10	66350666	66350667	A	G	7	GENIC	homozygous	51479543
10	66350926	66350927	T	-	4	GENIC	homozygous	52763988
10	66351483	66351484	C	T	26	GENIC	homozygous	51479547
10	66351618	66351619	A	G	13	GENIC	homozygous	52996226
10	66352061	66352062	T	A	24	GENIC	possibly homozygous	51479548
10	66352225	66352226	G	A	11	GENIC	homozygous	51479549
10	66353403	66353404	C	T	16	GENIC	possibly homozygous	52996228
10	66353719	66353720	C	T	4	GENIC	homozygous	51479554
10	66354075	66354076	T	TG	3	GENIC	homozygous	51479559
10	66354730	66354731	G	A	5	GENIC	homozygous	52996230
10	66354736	66354737	A	G	5	GENIC	homozygous	51479562
10	66355017	66355018	A	-	3	GENIC	homozygous	51479566
10	66355199	66355200	A	AG	2	GENIC	homozygous	51678706
10	66355219	66355220	G	A	8	GENIC	possibly homozygous	52996232
10	66355372	66355373	T	TA	5	GENIC	heterozygous	51479568
10	66355388	66355389	T	TAA	1	GENIC	homozygous	52564142
10	66355414	66355415	G	T	7	GENIC	homozygous	51479569