chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105499758	105499759	A	T	48	GENIC	homozygous	117031719
10	105500079	105500080	C	T	61	GENIC	homozygous	116836860
10	105500208	105500209	G	C	67	GENIC	homozygous	116836862
10	105500381	105500382	T	C	52	GENIC	homozygous	116836864
10	105500429	105500434	CTCGA		54	GENIC	homozygous	131470456
10	105501050	105501051	G	A	70	GENIC	homozygous	116836866
10	105501290	105501291	T	C	56	GENIC	homozygous	117031721
10	105501498	105501499	C	T	61	GENIC	homozygous	117031723
10	105502229	105502230	C	G	59	GENIC	possibly homozygous	117031725
10	105502416	105502417	C	A	50	GENIC	homozygous	117031727
10	105502752	105502753	C	T	47	GENIC	homozygous	116836868
10	105503332	105503333	C	T	77	GENIC	homozygous	116836870
10	105504401	105504402	A	C	19	GENIC	homozygous	116836872