chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	128435821	128435822	G	A	20	GENIC	homozygous	108332006
X	128437301	128437302	A	G	23	GENIC	homozygous	108332008
X	128437884	128437885	T	C	17	GENIC	homozygous	108332010
X	128440980	128440981	T	C	18	GENIC	homozygous	108332012
X	128443267	128443268	A	G	22	GENIC	homozygous	108332014
X	128443720	128443721	C	A	32	GENIC	homozygous	108332016
X	128445673	128445674	C	T	25	GENIC	homozygous	108332019
X	128447089	128447090	G	A	29	GENIC	homozygous	108332021
X	128447967	128447968	G	A	22	GENIC	homozygous	108332023
X	128449215	128449216	C	T	21	GENIC	homozygous	108332025
X	128450408	128450409	C	T	17	GENIC	homozygous	108332027
X	128451628	128451629	G	A	40	GENIC	homozygous	108332029
X	128452566	128452567	A	G	24	GENIC	homozygous	108332031
X	128452712	128452713	A	G	30	GENIC	homozygous	108332033
X	128455314	128455315	A	G	28	GENIC	homozygous	108332035
X	128455486	128455487	G	A	18	GENIC	homozygous	108332037
X	128455588	128455589	T	C	21	GENIC	homozygous	108332039
X	128455645	128455646	G	T	15	GENIC	homozygous	108332041