chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64352067	64352068	C	CCTT	47	GENIC	homozygous	51476382
10	64352459	64352460	G	GA	24	GENIC	homozygous	51674165
10	64355154	64355159	CCCCC	-----	5	GENIC	heterozygous	51476383
10	64355155	64355159	CCCC	----	5	GENIC	heterozygous	51476384
10	64357703	64357704	A	AAAAC	14	GENIC	homozygous	51674169
10	64357723	64357724	C	T	39	GENIC	heterozygous	51674171
10	64357723	64357724	C	CAAACAAAT	35	GENIC	homozygous	51674173
10	64358697	64358698	A	T	46	GENIC	homozygous	51674175
10	64360239	64360240	T	G	40	GENIC	heterozygous	51904698
10	64360433	64360434	A	-	3	GENIC	homozygous	51674177
10	64363674	64363675	C	T	6	GENIC	homozygous	51674179
10	64363678	64363679	C	T	7	GENIC	homozygous	51674181
10	64363682	64363683	C	T	7	GENIC	heterozygous	51674183
10	64364026	64364027	T	G	60	GENIC	homozygous	51674185
10	64364282	64364283	G	A	44	GENIC	homozygous	51674187
10	64366279	64366280	G	A	41	GENIC	possibly homozygous	51674189
10	64366873	64366874	C	T	50	GENIC	possibly homozygous	51674191
10	64367367	64367368	A	G	36	GENIC	heterozygous	51674193
10	64367393	64367394	C	A	41	GENIC	heterozygous	52250915
10	64367509	64367510	G	A	40	GENIC	homozygous	51674195
10	64367786	64367787	A	-	47	GENIC	homozygous	51674197
10	64369860	64369861	A	AATGATGATG	18	GENIC	homozygous	51674199
10	64370234	64370235	A	G	66	GENIC	possibly homozygous	51674201
10	64370467	64370468	A	G	50	GENIC	homozygous	51674203
10	64370480	64370481	A	G	54	GENIC	homozygous	51674205
10	64371085	64371086	G	A	39	GENIC	heterozygous	51674207
10	64371087	64371088	G	GCACA	20	GENIC	homozygous	51476386
10	64371087	64371088	G	A	37	GENIC	heterozygous	51674209
10	64371109	64371110	G	A	34	GENIC	heterozygous	51476387
10	64371117	64371118	G	A	38	GENIC	heterozygous	51904717