chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	43543439	43543440	T	G	9	GENIC	homozygous	108672331
X	43544269	43544270	T	C	11	GENIC	homozygous	108672332
X	43545064	43545065	G	A	4	GENIC	homozygous	108672334
X	43545732	43545733	T	A	8	GENIC	homozygous	108672335
X	43546180	43546181	A	G	22	GENIC	heterozygous	120026935
X	43546947	43546948	T	C	18	GENIC	homozygous	120026936
X	43547603	43547604	T	C	9	GENIC	homozygous	108672336
X	43549940	43549941	T	C	10	GENIC	homozygous	108672337
X	43550381	43550382	G	A	160	GENIC	heterozygous	120026937
X	43555899	43555900	T	C	8	GENIC	homozygous	108672339
X	43556044	43556045	A	G	7	GENIC	homozygous	108672340
X	43559515	43559516	A	G	13	GENIC	homozygous	108672342
X	43560778	43560779	C	T	4	GENIC	homozygous	108672343
X	43547186	43547187	T	A	18	GENIC	homozygous	108706195
X	43548890	43548891	A	G	14	GENIC	homozygous	108706197
X	43551123	43551124	C	T	19	GENIC	homozygous	108706199
X	43556918	43556919	T	G	10	GENIC	homozygous	108706201
X	43553123	43553124	G	C	7	GENIC	homozygous	120049892
X	43553156	43553157	C	T	8	GENIC	homozygous	120049893
X	43553194	43553195	A	C	4	GENIC	homozygous	120049894
X	43553172	43553173	G	A	4	GENIC	homozygous	108819832
X	43570034	43570035	C	A	11	GENIC	homozygous	108672344
X	43570506	43570507	C	T	12	GENIC	homozygous	108672345
X	43570623	43570624	G	C	14	GENIC	homozygous	108487285
X	43570718	43570719	T	C	9	GENIC	homozygous	108672346
X	43573046	43573047	T	A	12	GENIC	homozygous	108487291
X	43573393	43573394	A	G	17	GENIC	homozygous	108487293
X	43573857	43573858	A	T	18	GENIC	homozygous	108672347
X	43575945	43575946	T	G	12	GENIC	homozygous	108672348
X	43576056	43576057	G	A	14	GENIC	heterozygous	120049900
X	43591690	43591691	T	G	15	GENIC	homozygous	108487303