chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64349761	64349762	C	CT	6	GENIC	heterozygous	51476380
10	64349761	64349762	C	CTTT	6	GENIC	heterozygous	52381530
10	64351150	64351151	G	GGA	21	GENIC	homozygous	51904686
10	64351215	64351216	A	AGGGGCTGGGGATTTAGCTCAGT	12	GENIC	homozygous	52381532
10	64351300	64351309	AAAAACAAG	---------	3	GENIC	heterozygous	52381534
10	64352004	64352005	G	A	32	GENIC	possibly homozygous	51904688
10	64352067	64352068	C	CCTT	32	GENIC	homozygous	51476382
10	64353443	64353444	G	A	36	GENIC	homozygous	51904690
10	64353781	64353782	G	A	31	GENIC	homozygous	51904692
10	64355449	64355450	G	GAAAAAAAGAACCA	6	GENIC	homozygous	52381538
10	64356071	64356072	G	A	31	GENIC	homozygous	51904694
10	64357703	64357704	A	AAAAC	23	GENIC	homozygous	51674169
10	64359343	64359344	T	C	19	GENIC	homozygous	51904696
10	64359782	64359783	T	TC	7	GENIC	homozygous	52381540
10	64360433	64360434	A	-	3	GENIC	heterozygous	51674177
10	64360682	64360683	A	G	21	GENIC	homozygous	51904700
10	64361446	64361447	G	A	33	GENIC	homozygous	51904702
10	64363206	64363207	G	GAA	11	GENIC	heterozygous	52381542
10	64363206	64363207	G	GA	11	GENIC	heterozygous	52320117
10	64366744	64366745	C	A	25	GENIC	homozygous	51904704
10	64367255	64367256	G	A	8	GENIC	homozygous	51904706
10	64367509	64367510	G	A	29	GENIC	homozygous	51674195
10	64369860	64369861	A	AATAATG	15	GENIC	homozygous	51904710
10	64370169	64370170	G	A	35	GENIC	homozygous	51904715
10	64370234	64370235	A	G	31	GENIC	homozygous	51674201
10	64370467	64370468	A	G	26	GENIC	homozygous	51674203
10	64370480	64370481	A	G	29	GENIC	homozygous	51674205
10	64371087	64371088	G	GCGCGCACACACA	7	GENIC	heterozygous	52381544
10	64371087	64371088	G	GCGCGCACACACACA	7	GENIC	heterozygous	52381546