chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	70855161	70855162	C	T	43	GENIC	homozygous	112075984
16	70855604	70855605	C	T	35	GENIC	homozygous	112075986
16	70855699	70855700	G	T	26	GENIC	homozygous	112075990
16	70855721	70855722	T	C	29	GENIC	homozygous	112075992
16	70855925	70855926	T	C	37	GENIC	homozygous	112075994
16	70856397	70856398	A	G	41	GENIC	homozygous	112075996
16	70856901	70856902	A	T	28	GENIC	homozygous	112075998
16	70858302	70858303	G	A	26	GENIC	homozygous	112076000
16	70858413	70858414	T	C	16	GENIC	homozygous	112076002
16	70858492	70858493	T	C	16	GENIC	homozygous	112076004
16	70858499	70858500	T	C	17	GENIC	homozygous	112076006
16	70859343	70859344	T	C	35	GENIC	homozygous	112076008
16	70859457	70859458	A	C	26	GENIC	homozygous	112132322
16	70859925	70859926	A	T	45	GENIC	homozygous	112076010
16	70860041	70860042	G	A	36	GENIC	homozygous	112076012
16	70860329	70860330	A	G	18	GENIC	homozygous	112076014
16	70861535	70861536	C	T	29	GENIC	homozygous	112076016
16	70861582	70861583	G	A	32	GENIC	heterozygous	119172440
16	70862128	70862129	T	G	35	GENIC	homozygous	112076020
16	70862175	70862176	A	G	33	GENIC	homozygous	112076022
16	70862566	70862567	A	G	21	GENIC	possibly homozygous	119172442
16	70862640	70862641	T	C	25	GENIC	homozygous	112076024
16	70863907	70863908	C	T	26	GENIC	homozygous	112076026
16	70864135	70864136	T	C	36	GENIC	homozygous	112076028
16	70865784	70865785	G	A	36	GENIC	homozygous	112076030
16	70868101	70868102	T	C	36	GENIC	homozygous	112076032
16	70868122	70868123	G	A	42	GENIC	homozygous	112076034
16	70868129	70868130	T	C	39	GENIC	homozygous	112076036
16	70868478	70868479	C	T	39	GENIC	homozygous	112076038
16	70868779	70868780	C	G	22	GENIC	homozygous	112076040