chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	53001351	53001352	T	A	11	GENIC	homozygous	55377849
5	53002263	53002264	T	G	10	GENIC	homozygous	58132686
5	53002796	53002797	T	G	9	GENIC	homozygous	58132688
5	53003230	53003231	G	A	13	GENIC	homozygous	55377851
5	53003536	53003537	T	C	13	GENIC	homozygous	55377852
5	53003555	53003556	T	A	14	GENIC	homozygous	55377853
5	53003620	53003621	C	G	12	GENIC	homozygous	55377854
5	53003642	53003643	C	A	12	GENIC	homozygous	55377855
5	53003749	53003750	C	G	8	GENIC	homozygous	55377856
5	53004202	53004203	G	A	7	GENIC	homozygous	55377857
5	53004205	53004206	T	C	7	GENIC	homozygous	55377858
5	53004376	53004377	T	C	8	GENIC	homozygous	55377860
5	53004927	53004928	T	G	13	GENIC	homozygous	55377861
5	53005289	53005290	C	T	16	GENIC	homozygous	55377862
5	53005594	53005595	T	C	9	GENIC	homozygous	55377863
5	53005942	53005943	G	GTGTGTGTC	15	GENIC	homozygous	55377864
5	53006427	53006428	T	TA	11	GENIC	homozygous	55377866
5	53008128	53008129	T	C	14	GENIC	homozygous	55377868
5	53008565	53008566	C	CAATG	13	GENIC	homozygous	55377869
5	53009269	53009270	G	A	13	GENIC	homozygous	55377870
5	53009332	53009333	T	C	16	GENIC	homozygous	55377871
5	53010983	53010984	A	-	9	GENIC	homozygous	55377872
5	53011384	53011386	TT	--	8	GENIC	homozygous	55377873
5	53011594	53011595	G	GGGA	8	GENIC	homozygous	55377874
5	53013210	53013211	C	CAG	9	GENIC	homozygous	55377876
5	53013895	53013896	C	T	23	GENIC	homozygous	55377877
5	53014169	53014170	T	C	10	GENIC	homozygous	55377878
5	53015368	53015369	T	C	14	GENIC	homozygous	55377885
5	53015911	53015912	G	GTGAGGCTCTGA	10	GENIC	homozygous	55377886
5	53017580	53017581	C	A	20	GENIC	homozygous	55377890
5	53017581	53017582	T	TA	20	GENIC	homozygous	55377891
5	53017663	53017664	A	C	20	GENIC	heterozygous	58132690
5	53017664	53017665	G	A	19	GENIC	heterozygous	58132692
5	53017691	53017692	T	TC	19	GENIC	heterozygous	55377892
5	53017696	53017697	A	C	18	GENIC	heterozygous	55377893
5	53017714	53017715	A	G	15	GENIC	heterozygous	55377894
5	53019198	53019199	G	A	7	GENIC	homozygous	55377898