chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	121218535	121218536	A	G	18	GENIC	homozygous	115858106
7	121222839	121222840	T	C	19	GENIC	homozygous	115858108
7	121223317	121223318	C	T	21	GENIC	homozygous	115858110
7	121226093	121226094	A	G	25	GENIC	homozygous	115858112
7	121227221	121227222	A	G	28	GENIC	homozygous	115858114
7	121227630	121227631	A	C	11	GENIC	homozygous	115858116
7	121227893	121227894	C	T	29	GENIC	homozygous	115858118
7	121229029	121229030	A	T	16	GENIC	homozygous	115858124
7	121229582	121229583	C	A	26	GENIC	homozygous	115858126
7	121231490	121231491	G	C	30	GENIC	homozygous	115858128
7	121231601	121231602	A	G	22	GENIC	homozygous	115858130
7	121221329	121221329		AC	32	GENIC	homozygous	128512707
7	121228566	121228566		ACAGAC	7	GENIC	homozygous	128512708
7	121228594	121228594		ACACAG	13	GENIC	possibly homozygous	128512709
7	121232041	121232041		TG	6	GENIC	heterozygous	128512711
7	121232087	121232088	C	T	7	GENIC	homozygous	122850915
7	121232840	121232841	G	A	15	GENIC	homozygous	115858134