chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	127716578	127716579	T	C	17	GENIC	homozygous	108223668
1	127716588	127716589	G	C	8	GENIC	homozygous	108223670
1	127716598	127716599	T	C	6	GENIC	homozygous	108223672
1	127716601	127716602	G	A	6	GENIC	homozygous	108223674
1	127721106	127721107	A	C	16	GENIC	homozygous	108223676
1	127736361	127736362	C	T	17	GENIC	heterozygous	108223680
1	127736370	127736371	A	G	18	GENIC	heterozygous	108223682
1	127736384	127736385	C	A	15	GENIC	heterozygous	108223684
1	127736393	127736394	T	G	17	GENIC	heterozygous	108223686
1	127736404	127736405	T	C	16	GENIC	heterozygous	108223688
1	127737479	127737480	C	A	27	GENIC	heterozygous	109047915
1	127746616	127746617	G	A	18	GENIC	heterozygous	108742407
1	127746633	127746634	A	G	19	GENIC	heterozygous	108223694
1	127758036	127758037	C	T	16	GENIC	homozygous	108223696
1	127767966	127767967	T	C	36	GENIC	heterozygous	109047916
1	127767976	127767977	A	G	40	GENIC	heterozygous	109047917
1	127767979	127767980	A	G	38	GENIC	heterozygous	109047918
1	127767981	127767982	T	G	39	GENIC	heterozygous	109047919
1	127771685	127771686	T	G	5	GENIC	homozygous	108223698