chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	56324272	56324273	T	TA	1	GENIC	homozygous	56905670
4	56324273	56324274	T	A	1	GENIC	homozygous	58334966
4	56325207	56325208	C	CT	1	GENIC	homozygous	58464545
4	56325423	56325429	TTGTTG	------	1	GENIC	homozygous	56905673
4	56325663	56325664	A	C	11	GENIC	homozygous	56905675
4	56325891	56325892	A	-	1	GENIC	homozygous	56905679
4	56325956	56325957	A	G	10	GENIC	possibly homozygous	56905680
4	56326052	56326053	G	GA	7	GENIC	heterozygous	56905681
4	56326271	56326272	G	A	13	GENIC	possibly homozygous	56905682
4	56326600	56326601	T	TC	4	GENIC	homozygous	56905683
4	56326610	56326611	C	A	6	GENIC	homozygous	56905684
4	56326880	56326881	C	T	8	GENIC	possibly homozygous	56905685
4	56327525	56327526	T	A	3	GENIC	homozygous	56905686
4	56327528	56327529	T	A	2	GENIC	homozygous	56905687
4	56327854	56327855	C	A	12	GENIC	homozygous	56905688
4	56328089	56328090	C	CT	5	GENIC	homozygous	56905689
4	56328855	56328856	T	TCA	4	GENIC	homozygous	56905690
4	56329036	56329037	G	A	22	GENIC	possibly homozygous	56905691
4	56329272	56329273	C	T	11	GENIC	homozygous	56905692
4	56330514	56330515	G	GA	2	GENIC	homozygous	56905693
4	56330537	56330538	T	C	6	GENIC	homozygous	56905694
4	56330595	56330596	G	A	15	GENIC	homozygous	56905695
4	56331035	56331036	G	A	9	GENIC	homozygous	56905696
4	56331997	56331998	G	GTT	1	GENIC	homozygous	56905697
4	56332369	56332370	T	C	5	GENIC	homozygous	56905698
4	56332380	56332381	C	A	5	GENIC	homozygous	56905699
4	56332398	56332399	T	C	6	GENIC	homozygous	56905700
4	56333451	56333452	A	T	6	GENIC	homozygous	56905702
4	56334057	56334058	C	T	24	GENIC	possibly homozygous	56905703