chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	63776223	63776224	A	G	38	GENIC	homozygous	116616464
10	63778203	63778204	C	A	33	GENIC	possibly homozygous	116616468
10	63779688	63779689	C	T	8	GENIC	possibly homozygous	117062162
10	63779868	63779869	A	C	8	GENIC	homozygous	117998296
10	63780397	63780398	A	C	21	GENIC	homozygous	117998297
10	63780563	63780564	G	T	14	GENIC	homozygous	117013227
10	63780987	63780988	G	T	3	GENIC	homozygous	117998300
10	63781042	63781043	C	G	11	GENIC	homozygous	117998302
10	63781206	63781207	G	T	17	GENIC	homozygous	117998303
10	63781360	63781361	A	C	5	GENIC	homozygous	117998304
10	63781483	63781484	G	T	6	GENIC	homozygous	117998305
10	63788709	63788710	G	C	20	GENIC	homozygous	116616486
10	63790620	63790621	A	C	33	GENIC	homozygous	116616490
10	63790671	63790672	T	C	49	GENIC	homozygous	116616492
10	63794532	63794533	G	C	33	GENIC	homozygous	117255900
10	63780048	63780049	G	T	19	GENIC	homozygous	117219632
10	63782586	63782587	C	G	26	GENIC	homozygous	116791573
10	63790876	63790877	A	G	18	GENIC	homozygous	116791575
10	63794492	63794493	A	C	27	GENIC	homozygous	116791577
10	63790548	63790549	A	T	13	GENIC	homozygous	117079964
10	63794196	63794197	C	T	25	GENIC	homozygous	117079967
10	63788855	63788856	C	T	15	GENIC	homozygous	118041280
10	63794519	63794520	G	C	29	GENIC	homozygous	117255898
10	63794661	63794662	G	T	17	GENIC	homozygous	116616496
10	63794741	63794742	G	C	13	GENIC	homozygous	116616498
10	63795014	63795015	T	C	21	GENIC	homozygous	116616502