chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	63098594	63098595	C	T	15	GENIC	homozygous	116614957
10	63098660	63098661	T	C	26	GENIC	homozygous	116614961
10	63099252	63099253	G	A	23	GENIC	homozygous	116614963
10	63099823	63099824	C	T	27	GENIC	homozygous	116614965
10	63100064	63100065	A	G	26	GENIC	homozygous	116614967
10	63100140	63100141	C	T	26	GENIC	homozygous	116940175
10	63101023	63101024	A	T	30	GENIC	homozygous	116614971
10	63101552	63101553	A	G	28	GENIC	homozygous	116614975
10	63101620	63101621	T	C	26	GENIC	homozygous	116940177
10	63101993	63101994	A	G	24	GENIC	homozygous	116940179
10	63102331	63102332	T	A	23	GENIC	homozygous	116940181
10	63102557	63102558	C	T	16	GENIC	homozygous	116940183
10	63103222	63103223	A	G	27	GENIC	homozygous	116614979
10	63104437	63104438	C	A	31	GENIC	homozygous	116940187
10	63104674	63104675	T	C	25	GENIC	homozygous	116614985
10	63105126	63105127	G	C	11	GENIC	homozygous	116614987
10	63105266	63105267	T	C	25	GENIC	homozygous	116614991
10	63108555	63108556	T	A	18	GENIC	homozygous	116940191
10	63108576	63108577	T	G	14	GENIC	homozygous	116614999
10	63116108	63116109	T	C	20	GENIC	homozygous	116615009
10	63117102	63117103	T	C	29	GENIC	homozygous	116940197
10	63122868	63122869	G	A	6	GENIC	homozygous	116940199
10	63125951	63125952	C	T	16	GENIC	possibly homozygous	116978513
10	63130114	63130115	T	C	30	GENIC	homozygous	116940201