chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	70500408	70500409	A	G	12	GENIC	homozygous	108273120
X	70500409	70500410	G	T	11	GENIC	homozygous	108273122
X	70500421	70500422	A		11	GENIC	homozygous	129753284
X	70500427	70500427		G	11	GENIC	homozygous	129753285
X	70501153	70501154	T	C	13	GENIC	homozygous	108273124
X	70515049	70515050	A	T	4	GENIC	homozygous	108608535
X	70515034	70515035	C	T	4	GENIC	homozygous	108608527
X	70515037	70515038	C	T	4	GENIC	homozygous	108608529
X	70515040	70515041	C	A	4	GENIC	homozygous	108608531
X	70515047	70515048	C	T	4	GENIC	homozygous	108608533
X	70515051	70515052	C	T	4	GENIC	homozygous	108608537
X	70515055	70515056	C	T	4	GENIC	homozygous	108608540
X	70515060	70515061	A	G	4	GENIC	homozygous	108608542
X	70515063	70515064	C	A	4	GENIC	homozygous	108608544
X	70515065	70515065		CTGGTG	4	GENIC	homozygous	129753286
X	70515072	70515072		CC	2	GENIC	homozygous	129753287
X	70525448	70525448		G	10	GENIC	homozygous	129753288
X	70530282	70530283	G	T	14	GENIC	homozygous	108273126
X	70546559	70546589	TGGAAGCAACCCCCAGTGTTGCTGATTATG		4	GENIC	homozygous	129753289
X	70553336	70553337	C	G	2	GENIC	homozygous	130200257