chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	78160906	78160907	T	G	65	GENIC	heterozygous	119929390
X	78161035	78161036	G	A	114	GENIC	heterozygous	120003768
X	78161197	78161198	G	A	68	GENIC	heterozygous	120054907
X	78161242	78161243	G	A	49	GENIC	heterozygous	120030755
X	78161245	78161246	C	G	47	GENIC	heterozygous	120030756
X	78161247	78161248	A	C	50	GENIC	heterozygous	120030757
X	78161285	78161286	T	G	53	GENIC	heterozygous	120030758
X	78164105	78164106	T	G	14	GENIC	homozygous	120054908
X	78166667	78166668	T	C	67	GENIC	heterozygous	119929399
X	78175909	78175910	G	A	117	GENIC	heterozygous	119929405
X	78175986	78175987	C	T	150	GENIC	heterozygous	119929406
X	78176032	78176033	C	T	97	GENIC	heterozygous	120042117
X	78176077	78176078	C	A	92	GENIC	heterozygous	120003769
X	78176106	78176107	C	A	86	GENIC	heterozygous	120003770
X	78177235	78177236	C	T	123	GENIC	heterozygous	119929410
X	78177248	78177249	A	G	129	GENIC	heterozygous	119929411
X	78177260	78177261	A	G	132	GENIC	heterozygous	120054909
X	78177331	78177332	A	T	148	GENIC	heterozygous	120054910
X	78177356	78177357	T	C	122	GENIC	heterozygous	119929412
X	78177363	78177364	G	T	126	GENIC	heterozygous	119929413
X	78177378	78177379	G	A	122	GENIC	heterozygous	120003771
X	78178092	78178093	A	G	67	GENIC	heterozygous	119929414
X	78178109	78178110	T	C	81	GENIC	heterozygous	120054911
X	78178175	78178176	G	A	108	GENIC	heterozygous	119929416