chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	35251385	35251386	G	A	36	GENIC	homozygous	50729040
11	35253597	35253598	G	A	37	GENIC	homozygous	50729041
11	35253664	35253670	TGTGTG	------	6	GENIC	heterozygous	51179629
11	35253666	35253670	TGTG	----	6	GENIC	heterozygous	51179630
11	35254178	35254179	T	G	34	GENIC	homozygous	50729044
11	35254393	35254394	T	C	37	GENIC	homozygous	50729045
11	35254806	35254807	C	T	36	GENIC	homozygous	50729046
11	35255037	35255038	T	TACACACACACAC	12	GENIC	heterozygous	51179631
11	35255037	35255038	T	TACACACACACACAC	12	GENIC	heterozygous	51179632
11	35255104	35255105	T	C	33	GENIC	homozygous	50729049
11	35255679	35255682	TTG	---	40	GENIC	homozygous	50729050
11	35257359	35257360	T	TGCATTAGCTCATTCAGACTTTTTTTATTATTTAAAGAGGAGAAG	5	GENIC	homozygous	51179633
11	35258848	35258849	G	GA	20	GENIC	homozygous	50729051
11	35258861	35258862	T	TA	25	GENIC	homozygous	50729052
11	35259715	35259716	T	A	26	GENIC	homozygous	50729053
11	35259874	35259875	A	AC	24	GENIC	possibly homozygous	50729054
11	35259977	35259978	G	GTT	19	GENIC	possibly homozygous	50729055
11	35259977	35259978	G	GT	19	GENIC	heterozygous	50923972
11	35260644	35260645	G	A	33	GENIC	homozygous	50729056
11	35261629	35261630	T	A	37	GENIC	homozygous	50729059
11	35261856	35261857	G	A	31	GENIC	possibly homozygous	50729060
11	35262739	35262740	A	T	28	GENIC	homozygous	50729061
11	35263346	35263347	G	A	28	GENIC	homozygous	50729062
11	35263533	35263534	A	T	20	GENIC	homozygous	50729063
11	35263689	35263690	G	A	35	GENIC	homozygous	50729064
11	35263783	35263784	T	G	31	GENIC	homozygous	50729065
11	35265411	35265412	G	A	41	GENIC	homozygous	50729067
11	35266186	35266187	C	CTT	5	GENIC	heterozygous	50729068
11	35266320	35266321	G	-	28	GENIC	homozygous	50729076
11	35266187	35266189	TT	--	5	GENIC	heterozygous	50729069
11	35266257	35266258	G	C	14	GENIC	homozygous	50729075
11	35266611	35266612	A	G	37	GENIC	homozygous	50729077
11	35268169	35268170	T	C	26	GENIC	homozygous	50729078