chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5613323	5613324	A	G	40	GENIC	homozygous	130036029
20	5615512	5615520	CCTGTGGC		37	GENIC	homozygous	129980274
20	5616571	5616572	C	T	27	GENIC	heterozygous	403680768
20	5616568	5616569	C		27	GENIC	heterozygous	403680765
20	5616568	5616569	C	G	27	GENIC	heterozygous	403680766
20	5616571	5616572	C		27	GENIC	heterozygous	403680767
20	5616572	5616573	C		27	GENIC	heterozygous	403680769
20	5616572	5616573	C	T	27	GENIC	heterozygous	403680770
20	5616573	5616574	C		27	GENIC	heterozygous	403680771
20	5616573	5616574	C	T	27	GENIC	heterozygous	403680772
20	5616651	5616652	G	A	31	GENIC	homozygous	130036030
20	5617335	5617336	T		30	GENIC	homozygous	129980275
20	5617360	5617363	CTC		39	GENIC	homozygous	129980276
20	5617866	5617867	C	T	40	GENIC	homozygous	130036031
20	5617972	5617973	T	C	37	GENIC	homozygous	130036032
20	5618360	5618361	C	T	38	GENIC	homozygous	130036033
20	5618572	5618573	C		37	GENIC	homozygous	129980277