chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	104912717	104912718	T	C	16	GENIC	heterozygous	120007781
X	104912739	104912740	C	T	15	GENIC	heterozygous	120007782
X	104912769	104912770	G	T	14	GENIC	heterozygous	120007783
X	104912780	104912781	T	C	12	GENIC	heterozygous	120007784
X	104912785	104912786	G	A	12	GENIC	heterozygous	120007785
X	104912787	104912788	C	T	12	GENIC	heterozygous	120007786
X	104912920	104912921	G	A	22	GENIC	heterozygous	120106760
X	104912923	104912924	C	G	20	GENIC	heterozygous	120106761
X	104912966	104912967	C	T	31	GENIC	heterozygous	120097146
X	104912974	104912975	C	T	35	GENIC	heterozygous	120097147
X	104912991	104912992	A	T	41	GENIC	heterozygous	119942612
X	104913003	104913004	A	G	38	GENIC	heterozygous	119942613
X	104913009	104913010	G	T	34	GENIC	heterozygous	119942614
X	104913042	104913043	C	G	33	GENIC	heterozygous	119942616
X	104927339	104927340	T	C	12	GENIC	homozygous	108307897
X	104926063	104926064	G	T	10	GENIC	homozygous	108409777
X	104926065	104926066	G	T	10	GENIC	homozygous	108409779