chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	121054275	121054276	A	T	5	GENIC	homozygous	125135004
X	121054857	121054858	C	T	11	GENIC	homozygous	125115151
X	121056148	121056149	C	T	4	GENIC	heterozygous	125135005
X	121056149	121056150	G	A	4	GENIC	heterozygous	125135006
X	121057928	121057929	T	C	5	GENIC	homozygous	125115155
X	121058116	121058117	A	C	17	GENIC	homozygous	125135007
X	121058356	121058357	C	T	7	GENIC	homozygous	125135008
X	121060019	121060020	G	A	7	GENIC	homozygous	125135009
X	121060318	121060319	T	C	8	GENIC	homozygous	125115157
X	121060578	121060579	A	C	9	GENIC	homozygous	125135010
X	121062270	121062271	T	C	6	GENIC	homozygous	125135011
X	121062757	121062758	A	G	11	GENIC	homozygous	125135012
X	121063889	121063890	C	A	5	GENIC	homozygous	125135013
X	121063971	121063972	A	G	5	GENIC	homozygous	125135014
X	121064459	121064460	G	A	12	GENIC	homozygous	125135015
X	121064510	121064511	C	A	15	GENIC	homozygous	125135016
X	121064761	121064762	A	G	6	GENIC	homozygous	125135017
X	121064774	121064775	A	G	9	GENIC	homozygous	125115159
X	121065191	121065192	G	A	6	GENIC	homozygous	125135018
X	121065397	121065398	T	C	9	GENIC	homozygous	125115160
X	121065614	121065615	G	A	6	GENIC	homozygous	125135019
X	121066142	121066143	G	A	8	GENIC	homozygous	125115161
X	121066214	121066215	C	T	11	GENIC	homozygous	125135020
X	121066305	121066306	A	G	7	GENIC	homozygous	125115162
X	121066516	121066517	T	C	8	GENIC	homozygous	125115164
X	121066522	121066523	G	A	8	GENIC	homozygous	125135021
X	121066619	121066620	C	A	6	GENIC	homozygous	125135022
X	121066670	121066671	G	T	12	GENIC	homozygous	125135023