chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	117174101	117174102	A	G	28	GENIC	homozygous	140688980
X	117179159	117179160	T	C	34	GENIC	homozygous	140688981
X	117181113	117181114	A	G	23	GENIC	homozygous	140688982
X	117188004	117188005	A	C	30	GENIC	homozygous	140688983
X	117190887	117190888	C	T	28	GENIC	homozygous	140688984
X	117197522	117197523	T	C	33	GENIC	homozygous	140688985
X	117198712	117198713	A	G	24	GENIC	homozygous	140688986
X	117199458	117199459	A	C	32	GENIC	possibly homozygous	140688987
X	117199966	117199967	A	G	29	GENIC	homozygous	140688988
X	117200994	117200995	C	G	22	GENIC	homozygous	140688989
X	117201665	117201666	T	C	33	GENIC	homozygous	140688990
X	117202897	117202898	C	T	39	GENIC	homozygous	140688991
X	117203362	117203363	G	A	39	GENIC	homozygous	140688992
X	117204583	117204584	T	A	35	GENIC	homozygous	140688993
X	117205109	117205110	G	A	36	GENIC	homozygous	140688994
X	117207272	117207276	CACT		31	GENIC	homozygous	140594058
X	117184568	117184569	A		24	GENIC	possibly homozygous	140594054
X	117205236	117205236		ACCTGATGTCA	29	GENIC	homozygous	140594055
X	117206957	117206957		A	22	GENIC	homozygous	140594056
X	117207010	117207010		T	27	GENIC	homozygous	140594057
X	117207277	117207279	AC		31	GENIC	homozygous	140594059
X	117207280	117207281	G	C	31	GENIC	homozygous	140688995
X	117209230	117209231	G	A	28	GENIC	homozygous	140688996
X	117209436	117209437	C	T	40	GENIC	homozygous	140688997
X	117210503	117210504	A		23	GENIC	possibly homozygous	140594060
X	117212830	117212831	A	G	17	GENIC	homozygous	140688998
X	117213253	117213254	T	G	33	GENIC	possibly homozygous	140688999
X	117213766	117213767	A	G	31	GENIC	homozygous	140689000
X	117215612	117215613	C	T	26	GENIC	homozygous	140689001
X	117217410	117217411	G	A	18	GENIC	homozygous	140689004
X	117215884	117215885	C	T	34	GENIC	homozygous	140689002
X	117216678	117216679	T	A	42	GENIC	homozygous	140689003