chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9792829	9792830	A	G	50	GENIC	homozygous	111443612
3	9793303	9793304	T	G	48	GENIC	possibly homozygous	111443615
3	9794228	9794229	T	G	34	GENIC	homozygous	111443616
3	9794262	9794263	G	A	34	GENIC	homozygous	111443617
3	9794443	9794444	A	G	30	GENIC	homozygous	111443618
3	9794460	9794461	C	T	29	GENIC	homozygous	111443619
3	9794746	9794747	T	C	47	GENIC	homozygous	111443620
3	9794756	9794757	T	C	46	GENIC	homozygous	111443621
3	9794903	9794904	T	C	54	GENIC	homozygous	111443622
3	9795064	9795065	C	T	39	GENIC	homozygous	111443623
3	9795377	9795378	T	C	44	GENIC	homozygous	111443625
3	9795479	9795480	C	T	53	GENIC	homozygous	111443627
3	9795489	9795490	C	G	50	GENIC	homozygous	111443628
3	9796272	9796273	T	C	43	GENIC	homozygous	111443630
3	9796296	9796297	A	T	36	GENIC	homozygous	111443631
3	9796383	9796384	G	A	36	GENIC	homozygous	111443632
3	9796562	9796563	T	G	49	GENIC	homozygous	111443633
3	9796608	9796609	A	G	43	GENIC	homozygous	111443634
3	9796912	9796913	G	T	35	GENIC	possibly homozygous	111443635
3	9797087	9797088	T	C	48	GENIC	homozygous	111443636
3	9797203	9797204	G	A	42	GENIC	homozygous	111443637
3	9797339	9797340	C	T	40	GENIC	homozygous	111443638
3	9797487	9797488	A	G	35	GENIC	homozygous	111443639
3	9793327	9793328	G	C	52	GENIC	homozygous	119966886
3	9794586	9794587	C	T	38	GENIC	homozygous	119966887
3	9796764	9796764		C	40	GENIC	homozygous	127848648
3	9797556	9797559	ATC		29	GENIC	homozygous	127848649
3	9798146	9798147	C	T	36	GENIC	homozygous	111443640
3	9798348	9798349	A	C	42	GENIC	possibly homozygous	111443641
3	9798633	9798634	C	G	45	GENIC	homozygous	111443642
3	9798714	9798715	A	G	37	GENIC	homozygous	111443643
3	9798777	9798778	C	T	32	GENIC	homozygous	111443644