chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17056085	17056086	A	C	28	GENIC	homozygous	117983029
10	17056255	17056256	G	C	5	GENIC	homozygous	117983030
10	17056315	17056316	T	G	23	GENIC	homozygous	117983031
10	17056414	17056415	G	T	20	GENIC	homozygous	117983032
10	17056700	17056701	T	C	30	GENIC	homozygous	116739482
10	17056893	17056894	C	T	25	GENIC	homozygous	116917497
10	17057077	17057078	C	T	37	GENIC	homozygous	116917499
10	17057258	17057259	C	T	26	GENIC	homozygous	116917501
10	17057494	17057495	G	A	34	GENIC	homozygous	116917503
10	17057632	17057633	G	A	30	GENIC	possibly homozygous	116917505
10	17058216	17058217	C	T	34	GENIC	homozygous	116917507
10	17059545	17059546	T	C	34	GENIC	homozygous	116739485
10	17060071	17060072	T	C	35	GENIC	homozygous	116739486
10	17060650	17060651	C	T	30	GENIC	homozygous	116739489
10	17060805	17060806	C	T	26	GENIC	homozygous	116917509
10	17062429	17062430	G	T	24	GENIC	homozygous	116917511
10	17062681	17062682	A	G	32	GENIC	homozygous	116500124
10	17066951	17066952	A	G	23	GENIC	homozygous	116917513
10	17067087	17067088	A	C	39	GENIC	homozygous	116917515
10	17067098	17067099	T	C	42	GENIC	homozygous	116500138
10	17068150	17068151	G	A	30	GENIC	homozygous	116917517
10	17068342	17068343	C	T	30	GENIC	homozygous	116917519
10	17068399	17068400	A	G	37	GENIC	homozygous	116917521
10	17069633	17069634	C	T	42	GENIC	homozygous	116917523
10	17070553	17070554	G	A	43	GENIC	homozygous	116917525
10	17070925	17070926	G	A	32	GENIC	homozygous	116500150
10	17073304	17073305	T	C	33	GENIC	homozygous	116500164
10	17073402	17073403	C	T	44	GENIC	homozygous	116917527
10	17073451	17073452	G	A	31	GENIC	homozygous	116917529
10	17074110	17074111	G	A	34	GENIC	homozygous	116917531