chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	159703910	159703911	T	C	10	GENIC	homozygous	108515200
X	159704918	159704919	C	G	11	GENIC	homozygous	108681859
X	159704970	159704971	C	G	15	GENIC	homozygous	108681860
X	159705254	159705255	G	A	12	GENIC	homozygous	108355464
X	159705374	159705375	C	T	6	GENIC	homozygous	108355466
X	159705880	159705881	T	C	7	GENIC	homozygous	108681861
X	159707465	159707466	A	G	14	GENIC	homozygous	108355468
X	159708024	159708025	A	G	13	GENIC	homozygous	108355470
X	159709077	159709078	G	A	11	GENIC	homozygous	108355472
X	159710314	159710315	G	A	9	GENIC	homozygous	108355474
X	159711476	159711477	G	A	6	GENIC	homozygous	108355476
X	159712372	159712373	T	C	12	GENIC	homozygous	108355478
X	159712457	159712458	A	G	9	GENIC	homozygous	108355480
X	159707426	159707426		T	8	GENIC	homozygous	129805640
X	159711191	159711191		TGTA	10	GENIC	possibly homozygous	129805641
X	159713695	159713695		A	13	GENIC	homozygous	129805642