chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105231068	105231069	A	G	14	GENIC	homozygous	52082571
10	105231454	105231455	A	G	12	GENIC	homozygous	52082575
10	105232414	105232415	C	T	14	GENIC	homozygous	52330749
10	105231692	105231693	T	C	15	GENIC	homozygous	52330744
10	105232095	105232096	C	G	6	GENIC	heterozygous	52330746
10	105232147	105232148	T	C	11	GENIC	heterozygous	52330747
10	105232433	105232434	A	G	9	GENIC	homozygous	52330751
10	105232498	105232499	C	T	22	GENIC	homozygous	52330753
10	105232554	105232555	G	A	9	GENIC	possibly homozygous	52330755
10	105232565	105232566	C	T	9	GENIC	homozygous	52330757
10	105232622	105232623	T	C	21	GENIC	heterozygous	52330759
10	105233593	105233594	G	A	10	GENIC	heterozygous	52330761
10	105233636	105233637	G	A	17	GENIC	homozygous	52330763
10	105233746	105233747	T	C	19	GENIC	homozygous	52330765
10	105233926	105233927	G	A	13	GENIC	homozygous	52330767
10	105233930	105233931	G	A	13	GENIC	homozygous	52330769
10	105234964	105234965	G	T	7	GENIC	heterozygous	52330771
10	105235038	105235039	C	G	11	GENIC	homozygous	52330773
10	105235277	105235278	T	C	17	GENIC	possibly homozygous	52330775