chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	5200760	5200761	C	T	61	GENIC	possibly homozygous	117161498
10	5200871	5200872	G	A	59	GENIC	possibly homozygous	117161500
10	5201508	5201509	T	C	44	GENIC	possibly homozygous	116474472
10	5201675	5201676	G	A	57	GENIC	homozygous	117161502
10	5201846	5201847	A	G	72	GENIC	homozygous	116474478
10	5201893	5201894	G	A	80	GENIC	homozygous	116474480
10	5202469	5202470	T	C	61	GENIC	homozygous	116474482
10	5202570	5202571	T	C	58	GENIC	homozygous	116474486
10	5203159	5203160	T	C	38	GENIC	homozygous	117161504
10	5203263	5203264	A	G	56	GENIC	homozygous	116474488
10	5203424	5203425	A	G	41	GENIC	homozygous	116474490
10	5203514	5203515	G	A	56	GENIC	homozygous	116474492
10	5205050	5205051	G	A	49	GENIC	homozygous	116474494
10	5205529	5205530	C	T	64	GENIC	homozygous	116474496
10	5206139	5206140	C	T	49	GENIC	homozygous	116474500
10	5206335	5206336	C	T	36	GENIC	homozygous	116474502
10	5206451	5206452	G	A	54	GENIC	homozygous	116474504
10	5206781	5206782	T	C	45	GENIC	homozygous	116474506
10	5207544	5207545	T	C	45	GENIC	homozygous	116474508
10	5207552	5207553	A	G	55	GENIC	possibly homozygous	116474510
10	5207636	5207637	C	T	65	GENIC	homozygous	117161506
10	5208181	5208182	A	G	46	GENIC	homozygous	116474512
10	5209159	5209160	G	A	64	GENIC	homozygous	116474514
10	5209204	5209205	C	G	71	GENIC	homozygous	116474516
10	5209297	5209298	C	T	66	GENIC	homozygous	116474518
10	5209645	5209646	T	C	55	GENIC	homozygous	117161508
10	5210009	5210010	C	T	56	GENIC	homozygous	116474520
10	5210172	5210173	A	C	52	GENIC	homozygous	116474522
10	5210270	5210271	C	T	47	GENIC	homozygous	117161510
10	5210464	5210465	G	A	66	GENIC	homozygous	116474524
10	5211248	5211249	G	A	64	GENIC	homozygous	116474526
10	5211453	5211454	T	C	51	GENIC	homozygous	116474528