chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105231068	105231069	A	G	31	GENIC	homozygous	52082571
10	105231129	105231130	A	T	11	GENIC	homozygous	52850382
10	105231241	105231242	A	ATGTGTGTGTG	9	GENIC	heterozygous	53029209
10	105231242	105231246	TGTG	----	9	GENIC	heterozygous	52767888
10	105231244	105231246	TG	--	9	GENIC	heterozygous	52462996
10	105231454	105231455	A	G	16	GENIC	homozygous	52082575
10	105231692	105231693	T	C	19	GENIC	homozygous	52330744
10	105232095	105232096	C	G	27	GENIC	homozygous	52330746
10	105232147	105232148	T	C	30	GENIC	homozygous	52330747
10	105232414	105232415	C	T	28	GENIC	homozygous	52330749
10	105232433	105232434	A	G	27	GENIC	homozygous	52330751
10	105232498	105232499	C	T	22	GENIC	homozygous	52330753
10	105232554	105232555	G	A	40	GENIC	homozygous	52330755
10	105232565	105232566	C	T	36	GENIC	homozygous	52330757
10	105232622	105232623	T	C	17	GENIC	homozygous	52330759
10	105232986	105232987	G	GTCTGTCTGTCTGTCTCTC	7	GENIC	homozygous	52850385
10	105233547	105233555	CACGCACG	--------	10	GENIC	homozygous	52850388
10	105233593	105233594	G	A	21	GENIC	homozygous	52330761
10	105233636	105233637	G	A	20	GENIC	homozygous	52330763
10	105233746	105233747	T	C	31	GENIC	homozygous	52330765
10	105233926	105233927	G	A	26	GENIC	homozygous	52330767
10	105233930	105233931	G	A	27	GENIC	homozygous	52330769
10	105234964	105234965	G	T	14	GENIC	homozygous	52330771
10	105235038	105235039	C	G	24	GENIC	homozygous	52330773
10	105235277	105235278	T	C	23	GENIC	homozygous	52330775