chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	96440548	96440549	G	A	18	INTERGENIC	homozygous	55402457
7	96440606	96440607	A	T	24	INTERGENIC	homozygous	55402460
7	96440753	96440754	C	T	31	INTERGENIC	homozygous	54211601
7	96440850	96440851	G	A	28	INTERGENIC	homozygous	54211602
7	96440864	96440865	T	A	29	INTERGENIC	homozygous	55630739
7	96440913	96440914	A	G	32	INTERGENIC	homozygous	55630741
7	96440934	96440935	G	A	29	INTERGENIC	homozygous	54211603
7	96440991	96440992	G	A	23	INTERGENIC	homozygous	55630743
7	96441081	96441082	A	G	27	INTERGENIC	homozygous	54211604
7	96441100	96441101	A	C	33	INTERGENIC	homozygous	54211605
7	96441188	96441189	T	C	17	INTERGENIC	homozygous	54211606
7	96441189	96441190	T	C	17	INTERGENIC	homozygous	54211607
7	96441947	96441948	G	GGTGTGTGTGT	3	INTERGENIC	homozygous	55733725
7	96445019	96445020	T	-	8	INTERGENIC	homozygous	54030294
7	96453633	96453635	TG	--	5	INTERGENIC	homozygous	55059233
7	96454160	96454161	C	T	29	INTERGENIC	homozygous	55678023
7	96454303	96454304	C	T	25	INTERGENIC	homozygous	55678025
7	96455776	96455777	A	AAG	23	INTERGENIC	homozygous	55678027
7	96455840	96455841	C	CTG	6	INTERGENIC	homozygous	55733728
7	96458675	96458676	C	T	29	INTERGENIC	homozygous	55678029
7	96460540	96460541	C	T	34	INTERGENIC	homozygous	55678031
7	96461870	96461871	A	G	26	INTERGENIC	homozygous	55678033
7	96462122	96462123	C	CATGT	9	INTERGENIC	possibly homozygous	54989675
7	96462515	96462516	A	ATG	4	INTERGENIC	heterozygous	54030297
7	96462563	96462564	G	GTGTGTGT	15	INTERGENIC	heterozygous	55630803
7	96463277	96463279	TC	--	11	INTERGENIC	heterozygous	55143997