chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	144282724	144282725	G	GT	8	GENIC	homozygous	45243617
X	144292802	144292803	G	GT	10	GENIC	homozygous	45243637
X	144321582	144321583	A	T	10	GENIC	homozygous	45243713
X	144321584	144321585	A	C	10	GENIC	homozygous	45243714
X	144322831	144322832	T	TC	14	GENIC	homozygous	45243720
X	144323072	144323073	C	A	21	GENIC	heterozygous	45243721
X	144334685	144334686	A	ATAAG	7	GENIC	homozygous	45243757
X	144334691	144334692	C	-	9	GENIC	homozygous	45243758
X	144348529	144348530	A	T	8	GENIC	homozygous	45243776
X	144354275	144354276	C	A	9	GENIC	homozygous	45243778
X	144355375	144355376	C	T	12	GENIC	homozygous	45243782
X	144355394	144355395	C	T	12	GENIC	homozygous	45243783
X	144381123	144381124	A	-	8	GENIC	homozygous	45243830
X	144423431	144423432	T	G	8	GENIC	homozygous	45243877
X	144430403	144430404	G	-	9	GENIC	homozygous	45243883
X	144323037	144323038	G	T	15	GENIC	heterozygous	45952405