chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	124130484	124130485	G	A	19	GENIC	homozygous	57648757
3	124130991	124130992	T	C	18	GENIC	heterozygous	57648759
3	124131132	124131133	G	GA	8	GENIC	homozygous	57648761
3	124132088	124132089	A	-	6	GENIC	heterozygous	58322345
3	124132473	124132474	T	C	23	GENIC	homozygous	57648765
3	124133287	124133288	C	T	13	GENIC	homozygous	57648767
3	124133812	124133813	T	C	19	GENIC	possibly homozygous	57648769
3	124133846	124133847	T	C	25	GENIC	homozygous	57648771
3	124134979	124134980	T	C	13	GENIC	homozygous	57648773
3	124136194	124136195	G	A	15	GENIC	homozygous	57648777
3	124136284	124136285	C	T	12	GENIC	heterozygous	57648779
3	124136618	124136619	A	G	17	GENIC	possibly homozygous	57648781
3	124136982	124136983	C	T	9	GENIC	homozygous	57648783
3	124136990	124136991	T	C	11	GENIC	possibly homozygous	57648785
3	124137337	124137338	T	C	13	GENIC	possibly homozygous	57648787
3	124137893	124137894	T	C	24	GENIC	homozygous	57648789
3	124138413	124138414	A	AT	4	GENIC	homozygous	57648795
3	124138709	124138710	C	T	15	GENIC	homozygous	57648797
3	124139265	124139266	T	C	20	GENIC	homozygous	57648799
3	124139288	124139289	G	A	14	GENIC	homozygous	57648801
3	124139445	124139446	A	C	19	GENIC	heterozygous	57648803
3	124140240	124140241	G	A	14	GENIC	homozygous	57648805
3	124140579	124140580	A	G	26	GENIC	possibly homozygous	57648807
3	124140997	124140998	A	G	11	GENIC	homozygous	57648809
3	124141007	124141008	C	CT	4	GENIC	heterozygous	57648811
3	124141200	124141201	A	AGGGT	4	GENIC	homozygous	57648813
3	124141214	124141215	A	G	3	GENIC	homozygous	57648815
3	124141219	124141220	G	GC	2	GENIC	homozygous	57648817
3	124141322	124141323	C	T	6	GENIC	heterozygous	57648819
3	124141348	124141349	T	C	1	GENIC	homozygous	57648823
3	124141542	124141543	T	C	15	GENIC	possibly homozygous	57648825
3	124141645	124141646	C	T	20	GENIC	possibly homozygous	57648827
3	124143558	124143559	G	A	10	GENIC	homozygous	58560030
3	124143501	124143502	C	T	13	GENIC	homozygous	58560029