chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	29081125	29081126	C	G	19	GENIC	homozygous	109158521
20	29136809	29136810	G	A	28	GENIC	homozygous	109158715
20	29136887	29136888	G	A	23	GENIC	homozygous	109158717
20	29160774	29160775	T	G	12	GENIC	homozygous	109158749
20	29160807	29160808	T	G	17	GENIC	homozygous	109158752
20	29160817	29160818	T	G	22	GENIC	homozygous	109158754
20	29166578	29166579	A	G	26	GENIC	homozygous	109158769
20	29166599	29166600	G	A	25	GENIC	homozygous	109310479
20	29166600	29166601	T	G	24	GENIC	homozygous	109310481
20	29166883	29166884	C	T	22	GENIC	homozygous	109158771
20	29186418	29186419	A	G	33	GENIC	homozygous	109158821
20	29186423	29186424	A	G	34	GENIC	homozygous	109158823
20	29186427	29186428	A	C	31	GENIC	homozygous	109158825
20	29186448	29186449	T	G	31	GENIC	homozygous	109158827
20	29186460	29186461	C	G	34	GENIC	homozygous	109158829
20	29186487	29186488	T	A	29	GENIC	homozygous	109158831
20	29186518	29186519	T	C	22	GENIC	homozygous	109158833
20	29186547	29186548	T	A	15	GENIC	homozygous	109158835
20	29197404	29197405	C	G	24	GENIC	homozygous	109158881