chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	79918259	79918260	G	T	40	GENIC	homozygous	111634794
3	79919228	79919229	G	A	44	GENIC	homozygous	111634795
3	79919601	79919602	A	T	39	GENIC	homozygous	111634796
3	79919736	79919737	T	C	51	GENIC	homozygous	111634797
3	79919850	79919851	C	A	41	GENIC	homozygous	111634798
3	79920946	79920947	G	T	51	GENIC	homozygous	111634799
3	79921175	79921176	G	A	68	GENIC	possibly homozygous	111634800
3	79921647	79921648	A	G	41	GENIC	homozygous	111634801
3	79922444	79922445	A	G	33	GENIC	homozygous	111634802
3	79926125	79926126	A	G	44	GENIC	homozygous	111634803
3	79927989	79927990	A	G	31	GENIC	homozygous	111634804
3	79928066	79928067	T	A	28	GENIC	homozygous	111634805
3	79928601	79928602	T	C	33	GENIC	heterozygous	111634806
3	79928639	79928640	C	T	41	GENIC	heterozygous	111634807
3	79929031	79929032	A	G	37	GENIC	homozygous	111634808
3	79929381	79929382	C	G	49	GENIC	homozygous	111634809
3	79929492	79929493	T	C	50	GENIC	possibly homozygous	111634810
3	79929584	79929585	A	G	44	GENIC	homozygous	111634811
3	79929587	79929588	C	T	43	GENIC	homozygous	111634812
3	79929660	79929661	G	A	42	GENIC	possibly homozygous	111634813
3	79929937	79929938	A	G	48	GENIC	homozygous	111634814
3	79930647	79930648	A	G	42	GENIC	homozygous	111634815
3	79932228	79932229	C	T	61	GENIC	homozygous	111634816
3	79932539	79932540	G	C	59	GENIC	homozygous	111634817
3	79934695	79934696	T	G	51	GENIC	homozygous	111634818
3	79934907	79934908	G	A	55	GENIC	homozygous	111634819
3	79935861	79935862	C	T	78	GENIC	homozygous	111634820
3	79935866	79935867	C	G	76	GENIC	possibly homozygous	111634821
3	79936065	79936066	A	G	41	GENIC	homozygous	111634822
3	79936593	79936594	A	G	60	GENIC	homozygous	111634823
3	79936733	79936734	T	C	60	GENIC	homozygous	111634824
3	79936900	79936901	A	G	67	GENIC	homozygous	111634825
3	79937453	79937454	C	T	23	GENIC	homozygous	111634826
3	79937468	79937469	C	G	21	GENIC	possibly homozygous	111634827