chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	79818580	79818581	A	T	14	GENIC	homozygous	108278828
X	79854655	79854656	G	T	25	GENIC	possibly homozygous	108278958
X	79854657	79854658	G	T	26	GENIC	homozygous	108278960
X	79854673	79854674	G	C	28	GENIC	homozygous	108278962
X	79854700	79854701	C	A	28	GENIC	homozygous	108278964
X	79872596	79872597	C	A	36	GENIC	homozygous	108279006
X	79872854	79872855	G	A	30	GENIC	homozygous	108279008
X	79873204	79873205	G	T	42	GENIC	homozygous	108450336
X	79873240	79873241	C	A	43	GENIC	homozygous	108279010
X	79873250	79873251	C	A	40	GENIC	homozygous	108279012
X	79873257	79873258	T	G	40	GENIC	homozygous	108279014
X	79873507	79873508	T	A	18	GENIC	homozygous	108279022
X	79873508	79873509	A	T	18	GENIC	homozygous	108279024
X	79872652	79872653	G	A	29	GENIC	homozygous	108393642
X	79854654	79854655	A	T	25	GENIC	possibly homozygous	108526652