chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	44693323	44693324	T	-	34	GENIC	homozygous	45574980
20	44693530	44693531	T	TTGC	20	GENIC	homozygous	45574981
20	44694025	44694026	A	AC	25	GENIC	possibly homozygous	45574982
20	44694319	44694320	G	GA	25	GENIC	homozygous	45574983
20	44694322	44694323	G	C	22	GENIC	possibly homozygous	45574984
20	44694500	44694501	A	G	40	GENIC	homozygous	45574985
20	44694619	44694620	A	-	22	GENIC	homozygous	45574986
20	44695328	44695329	C	G	14	GENIC	homozygous	45574987
20	44695335	44695336	T	G	9	GENIC	homozygous	45636743
20	44695336	44695337	T	G	9	GENIC	homozygous	45744190
20	44695337	44695338	T	C	9	GENIC	homozygous	45636744
20	44695338	44695339	T	A	9	GENIC	homozygous	45636745
20	44695339	44695340	T	G	9	GENIC	homozygous	45636746
20	44695341	44695342	T	G	9	GENIC	homozygous	45744191
20	44695431	44695432	T	C	11	GENIC	homozygous	45574989
20	44695439	44695440	C	T	10	GENIC	heterozygous	45574990
20	44695517	44695518	T	C	20	GENIC	homozygous	45574991
20	44695823	44695824	G	C	9	GENIC	possibly homozygous	45574992
20	44695950	44695951	T	-	15	GENIC	homozygous	45574993
20	44696216	44696217	T	-	38	GENIC	homozygous	45574994
20	44696357	44696358	G	GT	16	GENIC	homozygous	45574995
20	44696381	44696382	C	CT	14	GENIC	homozygous	45574996
20	44696620	44696621	C	CT	19	GENIC	heterozygous	45574997
20	44696638	44696639	A	G	44	GENIC	heterozygous	45574998
20	44696651	44696652	A	G	41	GENIC	homozygous	45574999
20	44696738	44696739	A	-	36	GENIC	possibly homozygous	45575000
20	44696955	44696956	C	T	40	GENIC	homozygous	45764644
20	44697094	44697095	T	-	13	GENIC	homozygous	45575001
20	44697113	44697114	T	-	8	GENIC	heterozygous	45575002
20	44698044	44698045	A	AT	30	GENIC	homozygous	45575003
20	44698072	44698073	C	-	30	GENIC	homozygous	45575004