chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	31143711	31143712	T	C	5	GENIC	homozygous	108250084
X	31144827	31144828	T	C	19	GENIC	homozygous	108250086
X	31148429	31148430	A	C	5	GENIC	homozygous	108250088
X	31154541	31154542	G	A	11	GENIC	homozygous	108250090
X	31154832	31154833	C	T	12	GENIC	homozygous	108250092
X	31158253	31158254	A	C	12	GENIC	homozygous	108250094
X	31160475	31160476	A	T	8	GENIC	homozygous	119913271
X	31171880	31171881	T	C	15	GENIC	homozygous	108250096
X	31172207	31172208	G	A	5	GENIC	homozygous	108250098
X	31177300	31177301	G	T	11	GENIC	homozygous	108250100
X	31177982	31177983	G	A	17	GENIC	homozygous	108250102
X	31181579	31181580	G	A	10	GENIC	homozygous	108250106
X	31172879	31172880	T	C	10	GENIC	homozygous	108478578