chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	7111636	7111637	G	A	49	GENIC	homozygous	136627813
3	7111761	7111762	C	T	59	GENIC	homozygous	136627814
3	7111991	7111992	T	C	55	GENIC	homozygous	136627815
3	7112452	7112453	C	T	62	GENIC	homozygous	136627816
3	7113454	7113455	T		50	GENIC	homozygous	136546081
3	7114814	7114815	T	C	46	GENIC	homozygous	136627820
3	7113569	7113570	A	G	34	GENIC	homozygous	136627817
3	7114195	7114196	G	C	51	GENIC	homozygous	136627818
3	7114810	7114811	A	G	45	GENIC	homozygous	136627819
3	7115286	7115287	T	C	52	GENIC	homozygous	136627821
3	7115744	7115745	G	A	71	GENIC	homozygous	136627822
3	7116178	7116179	T	G	61	GENIC	possibly homozygous	136627823
3	7116334	7116335	T	A	62	GENIC	homozygous	136627824
3	7116394	7116395	G	A	57	GENIC	homozygous	136627825
3	7117326	7117326		TTGTTTGTTTGT	36	GENIC	homozygous	136546082
3	7121766	7121767	G	A	53	GENIC	homozygous	136627826
3	7122564	7122565	C	A	56	GENIC	homozygous	136627827
3	7123394	7123395	G	A	68	GENIC	homozygous	136627828
3	7124869	7124870	G	C	57	GENIC	homozygous	136627829
3	7126404	7126405	A		5	GENIC	heterozygous	403056677
3	7126404	7126405	A	T	5	GENIC	heterozygous	403056678