chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59749651	59749652	A	G	21	GENIC	homozygous	116608663
10	59749941	59749942	G	A	16	GENIC	homozygous	116608665
10	59750116	59750117	A	G	36	GENIC	homozygous	116608667
10	59750816	59750817	C	T	31	GENIC	homozygous	116608669
10	59751972	59751973	T	C	21	GENIC	homozygous	116608671
10	59752533	59752534	C	G	20	GENIC	homozygous	116608673
10	59754879	59754880	A	G	27	GENIC	homozygous	116608675
10	59755896	59755897	T	A	24	GENIC	homozygous	116608677
10	59751249	59751249		AAG	23	GENIC	homozygous	128820910
10	59751356	59751363	CTGAACT		33	GENIC	homozygous	128820911
10	59752532	59752533	C		20	GENIC	homozygous	128820912
10	59756708	59756720	AGGGAGGGAGGG		19	GENIC	homozygous	128820913
10	59757443	59757444	T	C	16	GENIC	homozygous	116608679
10	59758702	59758703	G	A	19	GENIC	homozygous	116608681
10	59758918	59758919	A	G	17	GENIC	homozygous	116608683
10	59758947	59758948	A	G	20	GENIC	homozygous	116608685
10	59760146	59760147	T	C	21	GENIC	possibly homozygous	116788954
10	59760413	59760414	A	T	21	GENIC	homozygous	116608691
10	59760650	59760651	G	C	20	GENIC	homozygous	116608693
10	59761146	59761150	CTGT		22	GENIC	homozygous	128820914
10	59761293	59761294	A	G	20	GENIC	homozygous	116788955
10	59761384	59761385	T	C	23	GENIC	homozygous	117995656
10	59761389	59761390	C	G	20	GENIC	homozygous	117995657
10	59761393	59761393		T	19	GENIC	homozygous	128820915
10	59761433	59761434	G	A	20	GENIC	homozygous	117995658
10	59761895	59761896	G	T	11	GENIC	homozygous	116608695
10	59763265	59763266	G	A	25	GENIC	homozygous	116608697
10	59763411	59763412	T	C	22	GENIC	homozygous	116608699
10	59763568	59763568		G	17	GENIC	homozygous	128820916
10	59765951	59765951		T	24	GENIC	homozygous	128820917
10	59770583	59770584	C	A	20	GENIC	homozygous	116608701
10	59770639	59770640	C	A	22	GENIC	homozygous	116608703
10	59771440	59771441	T	C	12	GENIC	homozygous	116608705