chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64351150	64351151	G	GGA	11	GENIC	homozygous	51904686
10	64352004	64352005	G	A	11	GENIC	homozygous	51904688
10	64352067	64352068	C	CCTT	9	GENIC	possibly homozygous	51476382
10	64353443	64353444	G	A	27	GENIC	possibly homozygous	51904690
10	64353781	64353782	G	A	18	GENIC	possibly homozygous	51904692
10	64356071	64356072	G	A	23	GENIC	possibly homozygous	51904694
10	64357703	64357704	A	AAAAC	1	GENIC	homozygous	51674169
10	64359343	64359344	T	C	10	GENIC	possibly homozygous	51904696
10	64361446	64361447	G	A	22	GENIC	possibly homozygous	51904702
10	64366744	64366745	C	A	23	GENIC	homozygous	51904704
10	64367509	64367510	G	A	19	GENIC	homozygous	51674195
10	64369860	64369861	A	AATAATG	1	GENIC	homozygous	51904710
10	64370169	64370170	G	A	23	GENIC	possibly homozygous	51904715
10	64370234	64370235	A	G	25	GENIC	homozygous	51674201
10	64370467	64370468	A	G	10	GENIC	homozygous	51674203
10	64370480	64370481	A	G	12	GENIC	homozygous	51674205
10	64363206	64363207	G	GA	2	GENIC	heterozygous	52320117