chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	110016237	110016238	C	T	13	GENIC	homozygous	117423307
9	110017927	110017928	T	C	22	GENIC	homozygous	117642040
9	110019155	110019156	G	A	24	GENIC	homozygous	117642042
9	110020278	110020279	G	T	19	GENIC	homozygous	117642044
9	110023054	110023055	T	A	24	GENIC	homozygous	117642046
9	110023615	110023616	C	T	25	GENIC	homozygous	117642048
9	110023750	110023751	C	T	29	GENIC	homozygous	117642050
9	110024555	110024556	G	A	25	GENIC	homozygous	117423319
9	110026246	110026247	A	G	3	GENIC	homozygous	117642052
9	110027460	110027461	A	G	24	GENIC	possibly homozygous	117642054
9	110027473	110027474	C	T	28	GENIC	homozygous	117642056
9	110027505	110027506	G	A	26	GENIC	homozygous	117642058
9	110027970	110027971	T	C	23	GENIC	homozygous	117642060
9	110028719	110028720	C	G	26	GENIC	homozygous	117642062
9	110030654	110030655	C	G	24	GENIC	homozygous	117642066
9	110022670	110022671	C	T	26	GENIC	heterozygous	117776632
9	110022723	110022724	T	G	24	GENIC	possibly homozygous	117776634