chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	35250694	35250695	G	A	20	GENIC	homozygous	51581957
11	35252356	35252357	T	-	18	GENIC	possibly homozygous	51256224
11	35253006	35253007	G	A	12	GENIC	homozygous	51581959
11	35253007	35253008	G	A	12	GENIC	homozygous	51581961
11	35253664	35253670	TGTGTG	------	8	GENIC	homozygous	51179629
11	35254178	35254179	T	G	36	GENIC	homozygous	50729044
11	35254393	35254394	T	C	24	GENIC	homozygous	50729045
11	35254806	35254807	C	T	21	GENIC	homozygous	50729046
11	35255037	35255038	T	TAC	8	GENIC	possibly homozygous	51581963
11	35257359	35257360	T	TGCATTAGCTCATTCAGACTTTTTTTATTATTTAAAGAGGAGAAG	7	GENIC	homozygous	51179633
11	35259715	35259716	T	A	22	GENIC	homozygous	50729053
11	35260203	35260204	C	T	24	GENIC	homozygous	51581965
11	35260644	35260645	G	A	18	GENIC	homozygous	50729056
11	35260985	35261005	CGCGAGTGGGTATGTGCGCG	--------------------	3	GENIC	homozygous	51581967
11	35261629	35261630	T	A	14	GENIC	homozygous	50729059
11	35262739	35262740	A	T	19	GENIC	homozygous	50729061
11	35263783	35263784	T	G	22	GENIC	homozygous	50729065
11	35261778	35261779	G	-	15	GENIC	homozygous	51232333
11	35262402	35262403	C	T	23	GENIC	homozygous	51232334
11	35260925	35260926	C	CGT	2	GENIC	homozygous	51212336
11	35264652	35264653	T	C	14	GENIC	possibly homozygous	51581969
11	35266187	35266189	TT	--	4	GENIC	heterozygous	50729069
11	35266207	35266212	GGTTC	-----	13	GENIC	heterozygous	51179634
11	35266233	35266234	G	A	10	GENIC	homozygous	51581971
11	35266257	35266258	G	C	14	GENIC	homozygous	50729075
11	35266611	35266612	A	G	18	GENIC	homozygous	50729077
11	35266918	35266919	T	C	20	GENIC	homozygous	51232337
11	35268169	35268170	T	C	25	GENIC	homozygous	50729078
11	35268489	35268490	G	A	25	GENIC	homozygous	51581973
11	35271458	35271459	T	C	22	GENIC	homozygous	51232339