chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	217530778	217530779	A	G	34	GENIC	homozygous	59395354
2	217531441	217531442	C	T	38	GENIC	homozygous	59395355
2	217531761	217531762	C	T	37	GENIC	homozygous	59395356
2	217531850	217531851	C	T	33	GENIC	homozygous	59395357
2	217531938	217531939	C	CA	8	GENIC	heterozygous	59395358
2	217533101	217533102	A	T	18	GENIC	homozygous	59395359
2	217533487	217533488	C	CT	14	GENIC	heterozygous	59395360
2	217533487	217533488	C	CTT	14	GENIC	heterozygous	59774337
2	217534422	217534423	T	G	36	GENIC	homozygous	59395361
2	217535148	217535149	T	C	38	GENIC	possibly homozygous	59395363
2	217535275	217535276	G	C	23	GENIC	homozygous	59395364
2	217535389	217535390	T	C	40	GENIC	possibly homozygous	59395365
2	217536071	217536072	T	C	35	GENIC	homozygous	59395366
2	217536085	217536086	A	G	37	GENIC	homozygous	59395367
2	217536086	217536087	G	A	38	GENIC	homozygous	59395368
2	217536385	217536388	TTT	---	21	GENIC	possibly homozygous	59395369
2	217536586	217536587	C	CGTGTGT	15	GENIC	homozygous	59395370
2	217536836	217536837	C	T	30	GENIC	homozygous	59395371
2	217536923	217536924	C	T	33	GENIC	homozygous	59395372
2	217537424	217537425	T	C	42	GENIC	homozygous	59395373
2	217538354	217538355	G	A	39	GENIC	homozygous	59395374
2	217540938	217540939	T	C	26	GENIC	homozygous	59395375
2	217541440	217541441	C	CT	20	GENIC	homozygous	59395376
2	217541453	217541454	G	GT	20	GENIC	homozygous	59395377
2	217542272	217542273	T	C	39	GENIC	homozygous	59395378
2	217542661	217542662	A	G	26	GENIC	homozygous	59395379
2	217543304	217543305	A	T	34	GENIC	homozygous	59395380
2	217543447	217543448	T	G	43	GENIC	homozygous	59395381
2	217546112	217546113	G	T	25	GENIC	homozygous	59395382
2	217546433	217546434	A	AT	12	GENIC	homozygous	59395383
2	217546841	217546842	T	-	29	GENIC	homozygous	59395384