chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	17052522	17052523	T	C	14	GENIC	homozygous	116739472
10	17052789	17052790	T	C	32	GENIC	homozygous	116861115
10	17052832	17052833	T	C	29	GENIC	homozygous	116861117
10	17053958	17053959	A	G	18	GENIC	homozygous	116739473
10	17054034	17054035	A	G	26	GENIC	homozygous	116739474
10	17054037	17054038	G	A	27	GENIC	homozygous	116739475
10	17054067	17054068	A	T	28	GENIC	homozygous	116739476
10	17054249	17054250	G	C	19	GENIC	homozygous	116739477
10	17054475	17054476	C	T	18	GENIC	homozygous	116739478
10	17054663	17054664	G	A	21	GENIC	homozygous	116739479
10	17054802	17054803	G	A	23	GENIC	homozygous	116739480
10	17055223	17055224	C	A	15	GENIC	homozygous	116861119
10	17055739	17055740	C	T	23	GENIC	homozygous	116739481
10	17056987	17056988	T	C	11	GENIC	homozygous	116739484
10	17059545	17059546	T	C	17	GENIC	homozygous	116739485
10	17060071	17060072	T	C	15	GENIC	homozygous	116739486
10	17060085	17060086	C	T	13	GENIC	homozygous	116739487
10	17060110	17060111	C	T	15	GENIC	homozygous	116739488
10	17062681	17062682	A	G	7	GENIC	homozygous	116500124
10	17066962	17066963	C	T	23	GENIC	homozygous	116739490
10	17067098	17067099	T	C	20	GENIC	homozygous	116500138
10	17072817	17072818	C	T	19	GENIC	homozygous	116739491
10	17073304	17073305	T	C	19	GENIC	homozygous	116500164