chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	28449127	28449127		T	8	GENIC	homozygous	129730850
X	28449597	28449598	A	T	6	GENIC	homozygous	125102807
X	28450394	28450395	A	G	7	GENIC	homozygous	125102808
X	28450830	28450831	T	C	21	GENIC	homozygous	119912654
X	28461085	28461086	A	G	14	GENIC	homozygous	108248895
X	28459909	28459910	C	T	16	GENIC	homozygous	108377939
X	28460127	28460128	G	T	14	GENIC	homozygous	108377941
X	28459680	28459681	A	G	6	GENIC	homozygous	108248889
X	28460532	28460533	G	A	11	GENIC	homozygous	108248893
X	28462942	28462943	G	A	16	GENIC	homozygous	108377943
X	28463517	28463518	C	T	16	GENIC	homozygous	108377945
X	28464376	28464377	C	T	11	GENIC	homozygous	108377947
X	28464534	28464535	G	A	18	GENIC	homozygous	108248909
X	28465225	28465226	T	C	22	GENIC	homozygous	108248913
X	28465560	28465561	A	G	15	GENIC	homozygous	108248915
X	28465565	28465566	A	G	15	GENIC	homozygous	108248917
X	28464500	28464501	A		13	GENIC	homozygous	131239748
X	28468144	28468144		ATCC	28	GENIC	homozygous	129730855
X	28468321	28468322	T	G	14	GENIC	homozygous	108441600