chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	100489883	100489884	G	C	19	GENIC	homozygous	144089971
10	100490701	100490702	G	A	29	GENIC	homozygous	144089972
10	100490856	100490857	T	A	16	GENIC	homozygous	144089973
10	100492801	100492802	C	T	29	GENIC	homozygous	144089974
10	100493546	100493547	C	T	19	GENIC	possibly homozygous	144089975
10	100494136	100494137	G	A	25	GENIC	homozygous	144089976
10	100494479	100494480	A	G	26	GENIC	homozygous	144089977
10	100494669	100494670	C	T	23	GENIC	homozygous	144089978
10	100494712	100494714	TG		23	GENIC	homozygous	144079717
10	100494715	100494739	CGCCGTCAGTATCCAAGCCTACCA		23	GENIC	homozygous	144079718
10	100495981	100495982	G	A	24	GENIC	homozygous	144089979
10	100496276	100496276		CACCCCC	8	GENIC	homozygous	144079719
10	100496572	100496572		TTTTG	15	GENIC	homozygous	144079720
10	100496905	100496906	A	G	23	GENIC	homozygous	144089980
10	100496909	100496910	A	C	27	GENIC	homozygous	144089981
10	100498628	100498629	G	C	26	GENIC	homozygous	144089982
10	100501085	100501091	GTGTGC		12	GENIC	homozygous	144079721
10	100503429	100503430	G	A	24	GENIC	homozygous	144089983
10	100504672	100504673	T	C	14	GENIC	homozygous	144089984
10	100504797	100504798	C		26	GENIC	homozygous	144079722
10	100494712	100494713	T		23	GENIC	homozygous	404017393
10	100494712	100494713	T	C	23	GENIC	heterozygous	154670510
10	100495367	100495368	A	G	28	GENIC	homozygous	142265180
10	100504153	100504154	G	A	16	GENIC	homozygous	142265182
10	100504962	100504963	A	G	22	GENIC	homozygous	142265183
10	100504965	100504966	A	G	22	GENIC	homozygous	142265184
10	100504968	100504968		CCTCCT	21	GENIC	homozygous	142207538