chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5100829	5100830	A	G	15	GENIC	homozygous	109076786
20	5101112	5101113	G	A	36	GENIC	homozygous	109076789
20	5101197	5101198	G	A	23	GENIC	homozygous	109076793
20	5101399	5101400	A	G	21	GENIC	homozygous	109076795
20	5101582	5101583	C	T	25	GENIC	homozygous	109076797
20	5101741	5101742	T	C	18	GENIC	homozygous	109076799
20	5101750	5101751	C	T	21	GENIC	homozygous	109076801
20	5101830	5101831	A	G	13	GENIC	homozygous	109455485
20	5102061	5102062	A	G	31	GENIC	homozygous	109076803
20	5102220	5102221	A	G	33	GENIC	homozygous	109076807
20	5102245	5102246	T	C	35	GENIC	homozygous	109076809
20	5102403	5102404	T	C	43	GENIC	homozygous	109076811
20	5102577	5102578	T	C	43	GENIC	homozygous	109076813
20	5103305	5103306	C	T	19	GENIC	homozygous	109076815
20	5103313	5103314	C	T	19	GENIC	homozygous	109076817
20	5103549	5103550	A	G	20	GENIC	homozygous	109076819
20	5103699	5103700	A	G	24	GENIC	homozygous	109076823
20	5103796	5103797	A	G	33	GENIC	homozygous	109076825
20	5103847	5103848	C	T	36	GENIC	homozygous	109076827
20	5103887	5103888	G	T	37	GENIC	homozygous	109076829
20	5103910	5103911	G	A	46	GENIC	homozygous	109076831
20	5103941	5103942	A	C	39	GENIC	homozygous	109076833
20	5104299	5104300	G	A	24	GENIC	possibly homozygous	109076835
20	5104317	5104318	T	A	25	GENIC	homozygous	109076837
20	5104376	5104377	T	C	28	GENIC	possibly homozygous	109076839