chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	15350322	15350323	G	A	39	GENIC	homozygous	116498021
10	15350332	15350333	T	C	34	GENIC	homozygous	116498023
10	15362425	15362426	C	T	40	GENIC	homozygous	116498025
10	15362803	15362804	T	C	47	GENIC	homozygous	116498027
10	15363510	15363511	C	T	39	GENIC	homozygous	116498029
10	15363550	15363551	A	G	35	GENIC	homozygous	116498031
10	15363560	15363561	G	C	35	GENIC	homozygous	116498033
10	15365815	15365816	A	C	35	GENIC	homozygous	116498035
10	15365856	15365857	G	C	38	GENIC	homozygous	116498037
10	15366476	15366477	A	G	50	GENIC	homozygous	116498039
10	15368131	15368132	T	C	54	GENIC	homozygous	116498041
10	15375345	15375346	G	A	51	GENIC	homozygous	116498043
10	15375707	15375708	C	A	37	GENIC	homozygous	116498045
10	15375889	15375890	G	A	46	GENIC	homozygous	116498047
10	15376452	15376453	C	T	35	GENIC	heterozygous	117176941
10	15379837	15379838	T	C	48	GENIC	homozygous	116498049
10	15381379	15381380	C	T	37	GENIC	homozygous	116498051
10	15383097	15383098	G	T	43	GENIC	homozygous	116498053
10	15386941	15386942	T	C	61	GENIC	homozygous	116498055
10	15398577	15398578	T	G	24	GENIC	possibly homozygous	116498057
10	15402413	15402414	A	G	42	GENIC	homozygous	116498059
10	15403300	15403301	G	A	46	GENIC	homozygous	116498061
10	15358247	15358248	C	T	29	GENIC	heterozygous	117982622
10	15383217	15383218	A	G	27	GENIC	heterozygous	117982624
10	15383750	15383751	G	T	26	GENIC	homozygous	117982626
10	15383759	15383760	T	C	30	GENIC	possibly homozygous	117982628
10	15408945	15408946	G	T	21	GENIC	possibly homozygous	117982630