chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	145654584	145654585	C	A	21	GENIC	homozygous	143031843
3	145656202	145656203	A	G	28	GENIC	homozygous	143031844
3	145656623	145656637	GAGCTAAATCCCCA		11	GENIC	homozygous	143003360
3	145656747	145656748	C	G	16	GENIC	homozygous	143031845
3	145656748	145656749	C	T	15	GENIC	homozygous	143031846
3	145656833	145656834	T	C	23	GENIC	homozygous	143031847
3	145656902	145656903	A	G	21	GENIC	homozygous	143031848
3	145657348	145657349	C	A	21	GENIC	homozygous	143031849
3	145657724	145657724		C	19	GENIC	homozygous	143003361
3	145657767	145657768	G	A	22	GENIC	homozygous	143031850
3	145657964	145657965	A	G	21	GENIC	homozygous	143031851
3	145658004	145658005	T	G	24	GENIC	homozygous	143031852
3	145658068	145658069	C	T	22	GENIC	homozygous	143031853
3	145658223	145658224	A	C	14	GENIC	possibly homozygous	143031854
3	145658319	145658320	A	C	16	GENIC	homozygous	143031855
3	145658650	145658651	A	C	25	GENIC	homozygous	143031856
3	145658817	145658818	A	C	18	GENIC	homozygous	143031857
3	145659364	145659365	T	C	16	GENIC	homozygous	143031858
3	145661629	145661630	C	A	13	GENIC	homozygous	143031859
3	145661998	145661999	C	T	21	GENIC	homozygous	143031860
3	145662305	145662306	A	G	22	GENIC	homozygous	143031861
3	145662695	145662696	A	G	28	GENIC	homozygous	143031862
3	145663237	145663238	T	C	25	GENIC	homozygous	143031863
3	145663289	145663290	C	T	19	GENIC	homozygous	143031864
3	145663671	145663672	C	T	17	GENIC	homozygous	143031865
3	145666037	145666038	T	C	20	GENIC	homozygous	143031866
3	145667305	145667306	C	T	15	GENIC	homozygous	143031867
3	145667647	145667648	T	C	23	GENIC	homozygous	143031868