chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20531098	20531099	A	C	10	GENIC	possibly homozygous	47327908
16	20531592	20531593	A	G	16	GENIC	homozygous	48089357
16	20531619	20531620	A	G	16	GENIC	possibly homozygous	48089358
16	20531637	20531638	A	AC	24	GENIC	possibly homozygous	48089359
16	20531999	20532000	T	A	1	GENIC	homozygous	47740650
16	20532055	20532056	C	A	10	GENIC	possibly homozygous	48089360
16	20532943	20532944	A	G	9	GENIC	homozygous	47327912
16	20533104	20533105	T	C	18	GENIC	homozygous	48089361
16	20534167	20534168	G	A	16	GENIC	possibly homozygous	48089362
16	20534220	20534221	G	A	15	GENIC	homozygous	48089363
16	20534590	20534591	C	T	16	GENIC	possibly homozygous	48089364
16	20534855	20534856	C	-	2	GENIC	heterozygous	47327916
16	20536467	20536468	G	A	11	GENIC	possibly homozygous	48089365
16	20536650	20536651	A	G	13	GENIC	possibly homozygous	48089366
16	20536951	20536952	A	AAT	5	GENIC	homozygous	48089367
16	20536975	20536976	A	G	8	GENIC	homozygous	48089368
16	20537161	20537162	G	T	22	GENIC	possibly homozygous	48089369
16	20538465	20538466	T	C	10	GENIC	possibly homozygous	47327921
16	20538520	20538521	T	C	13	GENIC	homozygous	47327923
16	20538532	20538533	T	TAG	15	GENIC	homozygous	47327925
16	20539046	20539047	G	T	5	GENIC	heterozygous	47327927
16	20540560	20540562	TG	--	5	GENIC	heterozygous	47327929
16	20541582	20541583	G	A	2	GENIC	homozygous	47327931