chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39004283	39004284	G	A	22	GENIC	homozygous	116566031
10	39005975	39005976	C	T	26	GENIC	homozygous	116566033
10	39010108	39010109	G	T	17	GENIC	homozygous	116566035
10	39011677	39011678	C	T	35	GENIC	homozygous	116566037
10	39012509	39012510	T	C	27	GENIC	homozygous	116566039
10	39013782	39013783	G	A	31	GENIC	homozygous	116566041
10	39015909	39015910	G	A	16	GENIC	homozygous	116566043
10	39016149	39016150	G	A	25	GENIC	homozygous	116566045
10	39017846	39017847	A	G	32	GENIC	homozygous	116566047
10	39019868	39019869	T	C	21	GENIC	homozygous	116566049
10	39021853	39021854	G	A	21	GENIC	homozygous	116566051
10	39022969	39022970	A	G	34	GENIC	homozygous	116762842
10	39027972	39027973	T	A	27	GENIC	homozygous	116566053
10	39031478	39031479	A	T	24	GENIC	homozygous	116566057
10	39031835	39031836	T	C	21	GENIC	homozygous	116566059
10	39033738	39033739	T	C	11	GENIC	homozygous	116566061
10	39035971	39035972	A	G	31	GENIC	homozygous	116566063
10	39036711	39036712	G	A	21	GENIC	homozygous	116566065
10	39036935	39036936	T	G	30	GENIC	homozygous	116566067
10	39037450	39037451	A	T	22	GENIC	homozygous	116566069
10	39037957	39037958	T	C	28	GENIC	homozygous	116566071
10	39039155	39039156	T	G	15	GENIC	homozygous	116566073
10	39041005	39041006	G	A	22	GENIC	homozygous	116566075
10	39041527	39041528	T	C	27	GENIC	homozygous	116566077
10	39041615	39041616	C	G	22	GENIC	homozygous	116566079
10	39044449	39044450	T	C	34	GENIC	possibly homozygous	116566081
10	39050835	39050836	C	T	24	GENIC	homozygous	116566083
10	39051153	39051154	A	G	16	GENIC	homozygous	116566085
10	39052578	39052579	G	A	22	GENIC	homozygous	116566087
10	39052589	39052590	G	A	24	GENIC	homozygous	116566089
10	39053190	39053191	A	T	34	GENIC	homozygous	116566091