chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	24448133	24448134	C	-	11	INTERGENIC	homozygous	51095663
11	24448137	24448138	A	G	12	INTERGENIC	homozygous	50910388
11	24448174	24448175	A	AG	13	INTERGENIC	homozygous	50679071
11	24448195	24448196	G	A	15	INTERGENIC	homozygous	51095665
11	24448374	24448375	T	-	12	INTERGENIC	homozygous	50679072
11	24448563	24448564	T	TAAA	6	INTERGENIC	homozygous	51095667
11	24464567	24464569	TG	--	4	INTERGENIC	heterozygous	51176574
11	24484138	24484139	T	-	10	INTERGENIC	heterozygous	50910428
11	24523503	24523504	T	-	5	INTERGENIC	heterozygous	50679284
11	24525255	24525257	TA	--	5	INTERGENIC	homozygous	50679287
11	24525276	24525280	TTTT	----	5	INTERGENIC	homozygous	50679288
11	24531387	24531389	GT	--	12	INTERGENIC	possibly homozygous	51095675
11	24509532	24509533	A	-	22	INTERGENIC	heterozygous	51239683
11	24515130	24515131	A	AAG	2	INTERGENIC	homozygous	51239684
11	24529260	24529261	T	TCACA	12	INTERGENIC	heterozygous	51239685
11	24543050	24543052	TG	--	2	INTERGENIC	heterozygous	51239686
11	24560846	24560847	A	G	8	INTERGENIC	homozygous	50679411
11	24569507	24569508	C	CA	13	INTERGENIC	possibly homozygous	51239687
11	24573133	24573134	C	CA	28	INTERGENIC	heterozygous	50679436
11	24579695	24579696	G	A	16	INTERGENIC	homozygous	50679444
11	24579696	24579697	C	A	16	INTERGENIC	homozygous	50679445
11	24579707	24579708	C	G	12	INTERGENIC	homozygous	50679446
11	24579716	24579717	C	T	11	INTERGENIC	homozygous	50679447
11	24610927	24610928	C	CTT	2	INTERGENIC	homozygous	51095683