chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	20796314	20796315	C	T	27	GENIC	homozygous	117684380
9	20799169	20799170	C	A	16	GENIC	homozygous	117278701
9	20801470	20801471	C	G	21	GENIC	homozygous	117684382
9	20806095	20806096	A	G	5	GENIC	homozygous	117804528
9	20806096	20806097	C	A	5	GENIC	homozygous	117804529
9	20809956	20809957	G	C	19	GENIC	homozygous	117278731
9	20810385	20810386	T	G	17	GENIC	homozygous	117684388
9	20813398	20813399	G	A	20	GENIC	homozygous	117278735
9	20815691	20815692	C	T	16	GENIC	homozygous	117684390
9	20827215	20827216	T	C	10	GENIC	homozygous	117278779
9	20830900	20830901	A	G	14	GENIC	homozygous	117684392
9	20836236	20836237	T	C	23	GENIC	homozygous	117278798
9	20839791	20839792	T	C	28	GENIC	homozygous	117278802
9	20844066	20844067	C	A	13	GENIC	homozygous	117468646
9	20844067	20844068	A	T	13	GENIC	homozygous	117468647
9	20845302	20845303	T	C	16	GENIC	homozygous	117278816
9	20849172	20849173	C	A	18	GENIC	homozygous	117684394
9	20851265	20851266	A	G	16	GENIC	homozygous	117684396
9	20853332	20853333	A	G	12	GENIC	homozygous	117278840
9	20855135	20855136	T	C	29	GENIC	homozygous	117684398
9	20856788	20856789	C	G	32	GENIC	homozygous	117278845