chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	5200400	5200401	C	A	40	GENIC	homozygous	117161496
10	5200760	5200761	C	T	37	GENIC	homozygous	117161498
10	5200871	5200872	G	A	39	GENIC	homozygous	117161500
10	5201508	5201509	T	C	36	GENIC	homozygous	116474472
10	5201675	5201676	G	A	41	GENIC	homozygous	117161502
10	5201846	5201847	A	G	34	GENIC	homozygous	116474478
10	5201893	5201894	G	A	31	GENIC	homozygous	116474480
10	5202469	5202470	T	C	45	GENIC	homozygous	116474482
10	5202570	5202571	T	C	38	GENIC	homozygous	116474486
10	5203159	5203160	T	C	33	GENIC	homozygous	117161504
10	5203263	5203264	A	G	37	GENIC	homozygous	116474488
10	5203424	5203425	A	G	40	GENIC	homozygous	116474490
10	5203514	5203515	G	A	45	GENIC	homozygous	116474492
10	5205050	5205051	G	A	39	GENIC	homozygous	116474494
10	5205529	5205530	C	T	36	GENIC	homozygous	116474496
10	5206139	5206140	C	T	39	GENIC	homozygous	116474500
10	5206335	5206336	C	T	37	GENIC	homozygous	116474502
10	5206451	5206452	G	A	29	GENIC	homozygous	116474504
10	5206781	5206782	T	C	31	GENIC	homozygous	116474506
10	5207544	5207545	T	C	42	GENIC	homozygous	116474508
10	5207552	5207553	A	G	40	GENIC	homozygous	116474510
10	5207636	5207637	C	T	42	GENIC	homozygous	117161506
10	5208181	5208182	A	G	35	GENIC	homozygous	116474512
10	5209159	5209160	G	A	51	GENIC	homozygous	116474514
10	5209204	5209205	C	G	46	GENIC	homozygous	116474516
10	5209297	5209298	C	T	44	GENIC	homozygous	116474518
10	5209645	5209646	T	C	23	GENIC	homozygous	117161508
10	5210009	5210010	C	T	37	GENIC	homozygous	116474520
10	5210172	5210173	A	C	42	GENIC	homozygous	116474522
10	5210270	5210271	C	T	47	GENIC	homozygous	117161510
10	5210464	5210465	G	A	43	GENIC	homozygous	116474524
10	5211248	5211249	G	A	23	GENIC	homozygous	116474526
10	5211453	5211454	T	C	28	GENIC	homozygous	116474528