chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	107155059	107155060	T	C	11	GENIC	homozygous	403485871
X	107155059	107155060	T		11	GENIC	heterozygous	403485872
X	107155075	107155076	A	T	9	GENIC	homozygous	403485873
X	107155075	107155076	A		9	GENIC	heterozygous	403485874
X	107155083	107155084	A	T	8	GENIC	homozygous	403485875
X	107155083	107155084	A		8	GENIC	heterozygous	403485876
X	107155092	107155093	A	T	8	GENIC	homozygous	403485877
X	107155092	107155093	A	G	8	GENIC	heterozygous	403485878
X	107155092	107155093	A		8	GENIC	heterozygous	403485879
X	107235280	107235281	T		9	GENIC	heterozygous	142745729
X	107235280	107235281	T	A	9	GENIC	heterozygous	155200270
X	107248810	107248811	A		7	GENIC	heterozygous	403485880
X	107248810	107248811	A	T	7	GENIC	heterozygous	403485881
X	107248812	107248813	A		7	GENIC	heterozygous	403485882
X	107248812	107248813	A	T	7	GENIC	heterozygous	403485883
X	107351916	107351918	GT		15	GENIC	heterozygous	140591388
X	107267934	107267935	G		4	GENIC	homozygous	140591387
X	107255459	107255460	C	A	2	GENIC	homozygous	140676976