chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	99429743	99429744	C	T	22	GENIC	homozygous	116701626
10	99430416	99430417	C	T	29	GENIC	homozygous	116701628
10	99431521	99431522	T	C	25	GENIC	possibly homozygous	116907231
10	99431813	99431814	C	A	18	GENIC	homozygous	116907232
10	99432513	99432514	T	C	24	GENIC	homozygous	116701646
10	99433089	99433090	T	A	22	GENIC	homozygous	116907233
10	99433880	99433881	C	A	11	GENIC	homozygous	116907234
10	99434586	99434587	G	A	34	GENIC	homozygous	116907235
10	99434837	99434838	G	C	34	GENIC	homozygous	116907236
10	99434936	99434937	C	T	17	GENIC	homozygous	116907237
10	99435109	99435110	T	C	20	GENIC	homozygous	116701650
10	99435313	99435314	A	T	19	GENIC	homozygous	116907238
10	99435540	99435541	C	T	28	GENIC	homozygous	116907239
10	99435773	99435774	C	T	35	GENIC	homozygous	116907240
10	99435857	99435858	C	T	25	GENIC	homozygous	116907241
10	99437341	99437342	A	G	15	GENIC	homozygous	116907242
10	99437390	99437391	T	C	20	GENIC	homozygous	116907243
10	99438903	99438904	A	G	24	GENIC	homozygous	116701652
10	99439001	99439002	G	A	21	GENIC	homozygous	116701654
10	99439091	99439092	G	A	22	GENIC	homozygous	116701656
10	99439142	99439143	T	C	37	GENIC	homozygous	116701658
10	99440670	99440671	C	T	35	GENIC	homozygous	116907244
10	99440994	99440995	A	G	32	GENIC	homozygous	116701660
10	99440340	99440341	G	A	27	GENIC	heterozygous	118052145