chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20274699	20274700	G	-	33	GENIC	homozygous	47740306
16	20275128	20275130	CA	--	15	GENIC	homozygous	47740308
16	20275430	20275431	G	A	26	GENIC	possibly homozygous	47740309
16	20276021	20276022	T	C	33	GENIC	homozygous	47740311
16	20276259	20276260	G	T	28	GENIC	homozygous	47740313
16	20276799	20276800	T	C	18	GENIC	homozygous	47740315
16	20277206	20277207	A	G	26	GENIC	homozygous	47740317
16	20277697	20277698	T	C	31	GENIC	homozygous	47327032
16	20278114	20278115	C	T	33	GENIC	homozygous	47740319
16	20278278	20278279	A	G	34	GENIC	homozygous	47740321
16	20278518	20278519	A	G	43	GENIC	homozygous	47740322
16	20278654	20278655	T	-	19	GENIC	homozygous	47740324
16	20278776	20278777	G	T	24	GENIC	homozygous	47740326
16	20279046	20279049	GCA	---	29	GENIC	homozygous	47740328
16	20279256	20279260	GTGT	----	41	GENIC	homozygous	47740330
16	20279759	20279760	G	A	25	GENIC	homozygous	47740332