chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	9990371	9990372	T	C	13	GENIC	homozygous	111230356
17	9992169	9992170	T	G	13	GENIC	homozygous	111524422
17	9993333	9993334	G	A	24	GENIC	possibly homozygous	110953554
17	9996008	9996009	T	C	25	GENIC	homozygous	110953558
17	9996059	9996060	G	A	21	GENIC	homozygous	111524424
17	9996567	9996568	T	C	14	GENIC	homozygous	111230362
17	9997914	9997915	G	C	13	GENIC	homozygous	110953560
17	9999510	9999511	C	T	34	GENIC	homozygous	111524426
17	9999654	9999655	A	C	30	GENIC	possibly homozygous	111524428
17	9999881	9999882	G	A	20	GENIC	homozygous	111524430
17	9999922	9999923	A	G	20	GENIC	homozygous	111524432
17	9999996	9999997	A	G	11	GENIC	homozygous	111524434
17	10000201	10000202	T	C	12	GENIC	homozygous	110953564
17	10000288	10000289	G	A	25	GENIC	homozygous	111524436
17	10000386	10000387	G	A	20	GENIC	homozygous	111524438
17	10001134	10001135	T	C	17	GENIC	homozygous	111230370
17	10001442	10001443	A	T	14	GENIC	homozygous	111524440
17	10001700	10001701	T	C	33	GENIC	homozygous	111524442
17	10001711	10001712	A	G	28	GENIC	homozygous	110953566
17	10002158	10002159	T	C	25	GENIC	homozygous	110953570
17	10002390	10002391	G	A	25	GENIC	homozygous	111524444
17	10002508	10002509	G	A	21	GENIC	homozygous	111524446
17	10004231	10004232	G	C	3	GENIC	homozygous	110953577