chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	44313659	44313660	C	CTGCT	1	GENIC	homozygous	62255657
1	44313662	44313666	ATGA	----	2	GENIC	homozygous	62244505
1	44313723	44313724	A	AGTGCGCG	2	GENIC	homozygous	62225960
1	44313725	44313728	CAA	---	2	GENIC	homozygous	62225961
1	44313729	44313730	C	T	2	GENIC	homozygous	62225962
1	44313731	44313732	G	GC	1	GENIC	homozygous	62225963
1	44313733	44313734	T	TTA	1	GENIC	homozygous	62225964
1	44313735	44313736	T	TGGTG	1	GENIC	homozygous	62225965
1	44313863	44313864	T	C	9	GENIC	homozygous	60694731
1	44313868	44313869	A	C	10	GENIC	homozygous	60694732
1	44313884	44313888	TCAT	----	14	GENIC	homozygous	62125740
1	44313875	44313876	T	TTA	11	GENIC	homozygous	62125737
1	44313878	44313879	G	A	11	GENIC	homozygous	62125738
1	44313880	44313881	A	T	13	GENIC	homozygous	62125739
1	44313912	44313913	C	T	21	GENIC	homozygous	61290227
1	44313919	44313926	CCCTTGT	-------	23	GENIC	homozygous	60694735
1	44313952	44313953	G	T	28	GENIC	homozygous	60694739
1	44313963	44313964	G	T	30	GENIC	homozygous	60694740