chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	6595412	6595413	A	G	15	GENIC	homozygous	47717879
16	6596030	6596031	G	A	15	GENIC	homozygous	47797295
16	6596682	6596683	C	T	23	GENIC	homozygous	47255954
16	6597377	6597378	G	A	16	GENIC	homozygous	47797296
16	6597512	6597513	C	A	13	GENIC	homozygous	47797297
16	6598054	6598055	C	CGA	9	GENIC	homozygous	47255955
16	6598593	6598594	A	G	9	GENIC	homozygous	47717881
16	6599264	6599265	G	A	16	GENIC	homozygous	47717882
16	6599501	6599502	T	C	19	GENIC	homozygous	47717883
16	6599602	6599603	T	C	18	GENIC	homozygous	47255956
16	6600492	6600493	A	AG	14	GENIC	homozygous	47255957
16	6600498	6600499	A	G	16	GENIC	homozygous	47255958
16	6601014	6601015	A	C	15	GENIC	homozygous	47255959
16	6601016	6601017	C	A	14	GENIC	homozygous	47255960
16	6601333	6601334	T	C	9	GENIC	homozygous	47717884
16	6603672	6603673	T	TC	14	GENIC	homozygous	47255963
16	6603677	6603678	T	-	13	GENIC	homozygous	47255964
16	6603781	6603782	T	TCAACAA	8	GENIC	homozygous	47255966
16	6603992	6603993	C	CCAGAG	8	GENIC	homozygous	47255968
16	6605952	6605953	T	C	13	GENIC	homozygous	47255970
16	6607094	6607095	C	T	20	GENIC	homozygous	47255971
16	6608148	6608149	G	A	15	GENIC	homozygous	47255973
16	6608367	6608368	C	T	8	GENIC	homozygous	47797299
16	6608426	6608427	A	G	10	GENIC	homozygous	47255975
16	6608656	6608657	T	C	11	GENIC	homozygous	47255976