chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	44693323	44693324	T	-	14	GENIC	homozygous	45574980
20	44693530	44693531	T	TTGC	1	GENIC	homozygous	45574981
20	44694025	44694026	A	AC	14	GENIC	possibly homozygous	45574982
20	44694319	44694320	G	GA	8	GENIC	homozygous	45574983
20	44694322	44694323	G	C	9	GENIC	homozygous	45574984
20	44694500	44694501	A	G	6	GENIC	homozygous	45574985
20	44694620	44694621	A	-	4	GENIC	homozygous	45851156
20	44695823	44695824	G	C	1	GENIC	homozygous	45574992
20	44695950	44695951	T	-	2	GENIC	homozygous	45574993
20	44696216	44696217	T	-	15	GENIC	homozygous	45574994
20	44696357	44696358	G	GT	16	GENIC	homozygous	45574995
20	44696381	44696382	C	CT	19	GENIC	homozygous	45574996
20	44696620	44696621	C	CT	10	GENIC	heterozygous	45574997
20	44696638	44696639	A	G	13	GENIC	homozygous	45574998
20	44696651	44696652	A	G	10	GENIC	homozygous	45574999
20	44696738	44696739	A	-	22	GENIC	homozygous	45575000
20	44697094	44697095	T	-	17	GENIC	possibly homozygous	45575001
20	44697112	44697113	C	CTTTTT	8	GENIC	heterozygous	45859962
20	44697113	44697114	T	-	8	GENIC	heterozygous	45575002
20	44698044	44698045	A	AT	27	GENIC	possibly homozygous	45575003
20	44698072	44698073	C	-	26	GENIC	homozygous	45575004
20	44698731	44698732	G	GA	26	GENIC	homozygous	45575005