chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	14302697	14302698	G	T	16	GENIC	possibly homozygous	143406424
9	14302989	14302990	A	T	19	GENIC	homozygous	143406425
9	14304086	14304087	T	C	22	GENIC	homozygous	143406426
9	14304154	14304154		T	18	GENIC	heterozygous	141141689
9	14304694	14304695	G	A	29	GENIC	homozygous	143406427
9	14305156	14305157	T	C	22	GENIC	homozygous	143406428
9	14305573	14305574	G	A	24	GENIC	homozygous	143406429
9	14305660	14305661	T		26	GENIC	heterozygous	403627962
9	14305660	14305661	T	C	26	GENIC	homozygous	154563261
9	14307142	14307143	T		38	GENIC	homozygous	138448394
9	14307557	14307559	TG		33	GENIC	homozygous	138448395