chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	50343809	50343810	A	T	47	GENIC	heterozygous	138789318
10	50343901	50343902	A	G	55	GENIC	heterozygous	138789319
10	50348929	50348930	G	A	28	GENIC	homozygous	148057364
10	50359140	50359141	G	A	9	GENIC	homozygous	148057365
10	50355066	50355067	A	C	21	GENIC	heterozygous	403733049
10	50355085	50355086	G	C	21	GENIC	heterozygous	403733050
10	50355085	50355086	G	A	21	GENIC	heterozygous	403733051
10	50355089	50355090	A	C	22	GENIC	heterozygous	403733052
10	50370852	50370853	T	C	20	GENIC	homozygous	148057366
10	50402978	50402979	G	A	28	GENIC	homozygous	148057367
10	50408412	50408413	A	G	27	GENIC	homozygous	138789431
10	50408412	50408413	A		27	GENIC	heterozygous	403286184
10	50408418	50408419	A		28	GENIC	heterozygous	403286185
10	50408418	50408419	A	G	28	GENIC	homozygous	403286186
10	50408420	50408421	A		27	GENIC	heterozygous	403286187
10	50408420	50408421	A	G	27	GENIC	homozygous	403286188
10	50408427	50408428	G	T	29	GENIC	homozygous	138789432
10	50408427	50408428	G		29	GENIC	heterozygous	403286189
10	50432329	50432330	T	G	22	GENIC	homozygous	138789470
10	50435384	50435385	G		19	GENIC	homozygous	138683592
10	50373639	50373640	A		27	GENIC	homozygous	143431415
10	50362622	50362622		CA	32	GENIC	possibly homozygous	148047588
10	50426297	50426298	T		25	GENIC	homozygous	138683587
10	50430469	50430470	G		13	GENIC	homozygous	138683590
10	50437266	50437267	G	A	19	GENIC	homozygous	148057368
10	50443026	50443027	T		20	GENIC	possibly homozygous	138683598