chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	216759422	216759423	G	A	39	GENIC	possibly homozygous	109193542
1	216760179	216760180	G	A	33	GENIC	homozygous	109193544
1	216761714	216761715	A	G	40	GENIC	homozygous	108991962
1	216762800	216762801	G	A	33	GENIC	homozygous	109193546
1	216763297	216763298	C	T	35	GENIC	possibly homozygous	109193548
1	216763555	216763556	T	C	45	GENIC	possibly homozygous	108991963
1	216764373	216764374	G	T	30	GENIC	homozygous	109193550
1	216765879	216765880	G	T	40	GENIC	possibly homozygous	109193552
1	216766629	216766630	A	G	37	GENIC	homozygous	109193554
1	216766715	216766716	G	A	42	GENIC	possibly homozygous	109193556
1	216767436	216767437	C	T	44	GENIC	homozygous	109193558
1	216769863	216769864	G	T	39	GENIC	homozygous	108991965
1	216770643	216770644	T	C	29	GENIC	homozygous	108991966
1	216772229	216772230	T	C	46	GENIC	homozygous	109193560
1	216773276	216773277	A	T	27	GENIC	possibly homozygous	108991968
1	216775373	216775374	T	A	43	GENIC	homozygous	109193562
1	216775962	216775963	T	C	36	GENIC	homozygous	108991971
1	216776689	216776690	C	T	15	GENIC	possibly homozygous	109193564
1	216776705	216776706	C	T	39	GENIC	heterozygous	109193566
1	216777317	216777318	A	G	29	GENIC	possibly homozygous	108991974
1	216779579	216779580	A	G	34	GENIC	homozygous	109193568
1	216781907	216781908	C	T	40	GENIC	homozygous	109193570
1	216785878	216785879	A	C	22	GENIC	homozygous	108991993
1	216786463	216786464	A	T	32	GENIC	homozygous	109193572
1	216787366	216787367	G	T	42	GENIC	homozygous	109193574
1	216787672	216787673	A	G	43	GENIC	homozygous	108991995
1	216791196	216791197	C	T	23	GENIC	possibly homozygous	109193575
1	216792067	216792068	A	G	24	GENIC	homozygous	108992007
1	216792503	216792504	A	G	39	GENIC	homozygous	108992008
1	216796083	216796084	G	C	38	GENIC	homozygous	109193577
1	216796441	216796442	T	A	49	GENIC	possibly homozygous	108992025
1	216797474	216797475	G	A	38	GENIC	homozygous	108992030
1	216798024	216798025	C	T	29	GENIC	homozygous	109193579