chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39620616	39620617	G	A	33	GENIC	homozygous	116763128
10	39620747	39620748	G	A	20	GENIC	homozygous	116763130
10	39621052	39621053	A	G	30	GENIC	homozygous	116763138
10	39621881	39621882	A	G	19	GENIC	homozygous	116763148
10	39621993	39621994	G	A	19	GENIC	homozygous	116763152
10	39621307	39621308	G	T	15	GENIC	homozygous	117103383
10	39622113	39622114	G	T	8	GENIC	heterozygous	116763160
10	39622113	39622114	G	C	8	GENIC	heterozygous	117103385
10	39622135	39622136	C	T	13	GENIC	homozygous	116763162
10	39622168	39622169	T	C	18	GENIC	homozygous	116763166
10	39622299	39622300	G	A	25	GENIC	homozygous	116763176
10	39622378	39622379	A	G	17	GENIC	homozygous	117103387
10	39622528	39622529	T	C	28	GENIC	homozygous	116763178
10	39622579	39622580	G	A	34	GENIC	homozygous	116763180
10	39622616	39622617	G	A	29	GENIC	homozygous	116763182
10	39622678	39622679	A	G	22	GENIC	homozygous	116763184
10	39622778	39622779	C	A	25	GENIC	homozygous	116763186
10	39622853	39622854	C	T	24	GENIC	homozygous	116763188
10	39622447	39622448	C	T	20	GENIC	homozygous	117004928
10	39622455	39622456	T	C	21	GENIC	homozygous	117004930