chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	99429743	99429744	C	T	32	GENIC	homozygous	116701626
10	99430416	99430417	C	T	43	GENIC	homozygous	116701628
10	99430462	99430463	G	A	49	GENIC	possibly homozygous	116701630
10	99430463	99430464	G	A	49	GENIC	possibly homozygous	116701632
10	99431521	99431522	T	C	50	GENIC	homozygous	116907231
10	99431813	99431814	C	A	51	GENIC	homozygous	116907232
10	99432513	99432514	T	C	48	GENIC	homozygous	116701646
10	99433089	99433090	T	A	61	GENIC	possibly homozygous	116907233
10	99433880	99433881	C	A	41	GENIC	homozygous	116907234
10	99434586	99434587	G	A	77	GENIC	homozygous	116907235
10	99434837	99434838	G	C	69	GENIC	homozygous	116907236
10	99434936	99434937	C	T	67	GENIC	homozygous	116907237
10	99435109	99435110	T	C	61	GENIC	homozygous	116701650
10	99435313	99435314	A	T	62	GENIC	homozygous	116907238
10	99435540	99435541	C	T	64	GENIC	homozygous	116907239
10	99435773	99435774	C	T	61	GENIC	homozygous	116907240
10	99435857	99435858	C	T	91	GENIC	homozygous	116907241
10	99437341	99437342	A	G	77	GENIC	homozygous	116907242
10	99437390	99437391	T	C	64	GENIC	homozygous	116907243
10	99438903	99438904	A	G	60	GENIC	homozygous	116701652
10	99439001	99439002	G	A	58	GENIC	homozygous	116701654
10	99439091	99439092	G	A	64	GENIC	homozygous	116701656
10	99439142	99439143	T	C	60	GENIC	homozygous	116701658
10	99440074	99440075	C	G	42	GENIC	homozygous	118052144
10	99440340	99440341	G	A	44	GENIC	heterozygous	118052145
10	99440670	99440671	C	T	64	GENIC	homozygous	116907244
10	99440994	99440995	A	G	77	GENIC	homozygous	116701660