chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	61590764	61590765	G	A	22	GENIC	homozygous	56916623
4	61590786	61590787	T	C	20	GENIC	homozygous	56916624
4	61591132	61591133	A	C	23	GENIC	homozygous	56916625
4	61592142	61592143	G	A	25	GENIC	homozygous	56916626
4	61592379	61592380	A	G	25	GENIC	homozygous	56916627
4	61593235	61593237	AA	--	16	GENIC	heterozygous	56916628
4	61593236	61593237	A	-	16	GENIC	heterozygous	56916629
4	61594757	61594758	C	T	33	GENIC	homozygous	56916630
4	61595000	61595001	C	T	21	GENIC	homozygous	56916631
4	61595087	61595088	T	-	22	GENIC	homozygous	56916632
4	61595689	61595690	C	G	26	GENIC	homozygous	56916633
4	61596463	61596464	C	T	31	GENIC	homozygous	56916634
4	61597393	61597394	G	A	26	GENIC	homozygous	56916635
4	61597727	61597728	T	-	24	GENIC	heterozygous	56916636
4	61597731	61597738	TGTTGTG	-------	24	GENIC	heterozygous	56916637
4	61597737	61597738	G	GT	28	GENIC	homozygous	56916638
4	61598583	61598584	C	A	22	GENIC	homozygous	56916639
4	61598835	61598836	C	A	24	GENIC	homozygous	56916640
4	61599872	61599873	T	C	22	GENIC	homozygous	56916641