chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	135381884	135381885	C	T	14	GENIC	possibly homozygous	45483857
X	135382225	135382226	C	CACTT	5	GENIC	homozygous	45316198
X	135382379	135382380	G	T	10	GENIC	possibly homozygous	45483859
X	135397821	135397822	A	-	8	GENIC	homozygous	45316211
X	135398982	135398983	C	T	15	GENIC	homozygous	45316214
X	135402080	135402081	T	C	6	GENIC	heterozygous	45316218
X	135402746	135402747	A	-	9	GENIC	homozygous	45316220
X	135407340	135407341	T	C	11	GENIC	homozygous	45316227
X	135408602	135408603	C	CA	4	GENIC	homozygous	45234629
X	135409087	135409088	G	T	17	GENIC	possibly homozygous	45316229
X	135410559	135410560	A	G	5	GENIC	homozygous	45316231
X	135413959	135413960	G	T	21	GENIC	possibly homozygous	45316239