chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	99429743	99429744	C	T	38	GENIC	homozygous	116701626
10	99430416	99430417	C	T	26	GENIC	homozygous	116701628
10	99430462	99430463	G	A	30	GENIC	homozygous	116701630
10	99430463	99430464	G	A	29	GENIC	homozygous	116701632
10	99430540	99430541	C	A	24	GENIC	homozygous	116701634
10	99431318	99431319	G	C	44	GENIC	homozygous	116701636
10	99431366	99431367	G	A	46	GENIC	homozygous	116701638
10	99431402	99431403	G	A	58	GENIC	homozygous	116701640
10	99431633	99431634	A	C	34	GENIC	homozygous	116701642
10	99431877	99431878	C	G	53	GENIC	homozygous	116701644
10	99432513	99432514	T	C	64	GENIC	homozygous	116701646
10	99433637	99433638	G	T	6	GENIC	homozygous	116701648
10	99435109	99435110	T	C	28	GENIC	homozygous	116701650
10	99438903	99438904	A	G	45	GENIC	homozygous	116701652
10	99439001	99439002	G	A	47	GENIC	homozygous	116701654
10	99439091	99439092	G	A	44	GENIC	homozygous	116701656
10	99439142	99439143	T	C	44	GENIC	homozygous	116701658
10	99440994	99440995	A	G	53	GENIC	homozygous	116701660