chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	107155059	107155060	T	C	23	GENIC	homozygous	403485871
X	107155059	107155060	T		23	GENIC	heterozygous	403485872
X	107155075	107155076	A	T	17	GENIC	heterozygous	403485873
X	107155075	107155076	A		17	GENIC	heterozygous	403485874
X	107155083	107155084	A	T	19	GENIC	homozygous	403485875
X	107155083	107155084	A		19	GENIC	heterozygous	403485876
X	107155092	107155093	A	T	20	GENIC	homozygous	403485877
X	107155092	107155093	A	G	20	GENIC	heterozygous	403485878
X	107155092	107155093	A		20	GENIC	heterozygous	403485879
X	107212973	107212974	G	A	74	GENIC	heterozygous	142762452
X	107212985	107212986	C	T	71	GENIC	heterozygous	142762453
X	107213977	107213978	G	T	85	GENIC	heterozygous	142762455
X	107214082	107214083	A	G	76	GENIC	heterozygous	142762456
X	107212124	107212125	C	G	86	GENIC	heterozygous	147239306
X	107255470	107255471	T	C	22	GENIC	possibly homozygous	403485884
X	107255470	107255471	T		22	GENIC	heterozygous	141061798
X	107226088	107226090	AC		20	GENIC	heterozygous	140591386
X	107267934	107267935	G		7	GENIC	homozygous	140591387
X	107314666	107314667	C	T	29	GENIC	homozygous	149479362
X	107255459	107255460	C	A	22	GENIC	homozygous	140676976