chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	107963003	107963004	G	C	64	GENIC	homozygous	141525765
3	107965120	107965121	T	C	63	GENIC	homozygous	136784560
3	107965520	107965521	A	G	58	GENIC	homozygous	141525766
3	107966032	107966033	A	G	38	GENIC	homozygous	136784561
3	107966066	107966067	T	C	34	GENIC	homozygous	136784562
3	107966335	107966336	A	G	16	GENIC	homozygous	403073248
3	107966312	107966313	G		28	GENIC	heterozygous	403073245
3	107966312	107966313	G	A	28	GENIC	possibly homozygous	403073246
3	107966335	107966336	A		16	GENIC	heterozygous	403073247
3	107966362	107966363	A		11	GENIC	heterozygous	403073249
3	107966362	107966363	A	G	11	GENIC	homozygous	403073250
3	107969416	107969417	T	C	55	GENIC	homozygous	136784563
3	107969514	107969515	C	T	45	GENIC	homozygous	136784564
3	107970214	107970215	A	C	66	GENIC	homozygous	136784565
3	107970781	107970782	A	G	68	GENIC	homozygous	136784566
3	107971208	107971209	G	T	52	GENIC	homozygous	136784567
3	107971401	107971402	A	T	53	GENIC	homozygous	136784571
3	107971306	107971310	ATTT		42	GENIC	homozygous	136582627
3	107971382	107971383	T	C	52	GENIC	homozygous	136784568
3	107971384	107971385	A	T	53	GENIC	homozygous	136784569
3	107971399	107971400	C	A	53	GENIC	homozygous	136784570
3	107971408	107971409	G	T	52	GENIC	homozygous	136784572
3	107971419	107971420	T	A	52	GENIC	homozygous	136784573
3	107972055	107972056	T	C	35	GENIC	possibly homozygous	136784574
3	107972455	107972456	A	T	47	GENIC	homozygous	136784575
3	107972456	107972457	T	C	48	GENIC	homozygous	136784576
3	107972847	107972848	C	T	44	GENIC	homozygous	136784577
3	107973430	107973431	A	T	55	GENIC	homozygous	136784578