chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	27072383	27072384	T	C	12	GENIC	homozygous	131666124
6	27072400	27072401	G	A	13	GENIC	homozygous	132856773
6	27072404	27072405	C	T	14	GENIC	homozygous	132856774
6	27072655	27072656	T	G	4	GENIC	homozygous	132856775
6	27074011	27074012	T	C	12	GENIC	homozygous	132856776
6	27074293	27074293		G	9	GENIC	homozygous	128325006
6	27074263	27074277	AGACATAGTAGCCC		9	GENIC	homozygous	128325004
6	27074286	27074286		G	10	GENIC	homozygous	128325005
6	27079996	27079997	A	T	16	GENIC	possibly homozygous	132856778
6	27077101	27077102	A	G	24	GENIC	heterozygous	133825953
6	27079992	27079993	A	T	8	GENIC	possibly homozygous	132856777
6	27075964	27075970	ATGGCT		57	GENIC	homozygous	132850799
6	27076407	27076407		AAC	22	GENIC	homozygous	132850800
6	27078090	27078090		GA	49	GENIC	possibly homozygous	132850801
6	27079887	27079888	G		39	GENIC	homozygous	132850802
6	27076004	27076005	G	T	54	GENIC	homozygous	115449120
6	27078145	27078146	A	G	40	GENIC	homozygous	115449122