chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	63025250	63025251	A	C	23	GENIC	homozygous	51473903
10	63025375	63025377	GC	--	24	GENIC	homozygous	51902290
10	63025452	63025453	G	A	17	GENIC	homozygous	51473904
10	63025923	63025924	C	CAG	16	GENIC	homozygous	51902292
10	63026104	63026105	C	T	16	GENIC	homozygous	51473906
10	63026469	63026470	G	A	23	GENIC	homozygous	51902294
10	63026493	63026494	G	A	21	GENIC	homozygous	51902296
10	63036901	63036902	C	CTA	7	GENIC	possibly homozygous	51473926
10	63040222	63040230	AAAGAAAG	--------	1	GENIC	homozygous	52380833
10	63027171	63027176	TTTCT	-----	3	GENIC	heterozygous	52503592
10	63027757	63027758	T	-	9	GENIC	heterozygous	52380829
10	63046922	63046923	A	AGCTAAATCC	4	GENIC	homozygous	52380841
10	63046915	63046916	T	TG	3	GENIC	homozygous	52380835
10	63046918	63046919	T	TGCTAGGCAAGCGC	4	GENIC	homozygous	52380837
10	63046920	63046921	C	CTACCACT	4	GENIC	homozygous	52380839
10	63047747	63047748	C	T	18	GENIC	homozygous	51902300
10	63052370	63052371	A	-	6	GENIC	heterozygous	52995293
10	63053342	63053343	T	TTTGCAGGCATTTGGTTA	8	GENIC	possibly homozygous	51473945
10	63053596	63053597	G	T	26	GENIC	homozygous	51473946
10	63054810	63054812	CA	--	8	GENIC	heterozygous	52380845
10	63055462	63055464	GG	--	8	GENIC	heterozygous	51473948
10	63055463	63055464	G	-	8	GENIC	heterozygous	51473949
10	63055835	63055836	G	T	16	GENIC	homozygous	51473951
10	63055960	63055961	C	A	22	GENIC	homozygous	51473952
10	63056020	63056021	G	-	11	GENIC	homozygous	51473953
10	63056060	63056061	G	A	18	GENIC	homozygous	51473954
10	63058405	63058406	A	AGTGT	8	GENIC	heterozygous	52461012
10	63058418	63058420	GT	--	8	GENIC	heterozygous	52503596
10	63065162	63065164	GT	--	12	GENIC	homozygous	51987474
10	63075291	63075292	A	-	9	GENIC	homozygous	51671521
10	63081289	63081290	T	-	13	GENIC	heterozygous	51473987
10	63082412	63082413	T	TTATTG	7	GENIC	homozygous	52062871
10	63062170	63062172	CA	--	14	GENIC	heterozygous	52440365
10	63087790	63087791	G	A	12	GENIC	homozygous	51902306