chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	135474234	135474235	T	A	15	GENIC	heterozygous	130203191
X	135479688	135479689	C	T	14	GENIC	homozygous	108428249
X	135479724	135479725	C	G	8	GENIC	homozygous	108530342
X	135479742	135479743	A	G	7	GENIC	homozygous	108530344
X	135479729	135479730	C	G	7	GENIC	homozygous	108344209
X	135479731	135479732	C	G	6	GENIC	homozygous	108344211
X	135479760	135479761	A	G	6	GENIC	homozygous	108821376
X	135479754	135479755	A	G	7	GENIC	homozygous	108680816
X	135479783	135479784	G	C	5	GENIC	homozygous	120013139
X	135479788	135479789	G	C	5	GENIC	homozygous	120013140
X	135479789	135479790	G	C	5	GENIC	homozygous	120013141
X	135479791	135479792	G	C	5	GENIC	homozygous	120013142
X	135479794	135479795	G	C	5	GENIC	homozygous	120013143
X	135479786	135479787	T	C	5	GENIC	homozygous	108553313
X	135479817	135479818	G	C	7	GENIC	homozygous	108655314
X	135490370	135490370		G	7	GENIC	homozygous	129793857
X	135490380	135490380		T	7	GENIC	homozygous	129793858
X	135490385	135490386	G		7	GENIC	homozygous	129793859
X	135490390	135490390		T	7	GENIC	homozygous	129793860
X	135490410	135490411	A		9	GENIC	homozygous	129793861
X	135490439	135490440	C		10	GENIC	homozygous	129793862
X	135496004	135496004		T	10	GENIC	heterozygous	129793863
X	135507659	135507660	C		7	GENIC	homozygous	129793864