chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10362146	10362147	T	C	18	GENIC	homozygous	109090451
20	10362776	10362777	G	A	43	GENIC	homozygous	109237828
20	10363425	10363426	T	C	18	GENIC	homozygous	109090455
20	10363580	10363581	C	T	22	GENIC	homozygous	109237829
20	10368940	10368941	A	G	31	GENIC	homozygous	109237830
20	10369350	10369351	T	C	46	GENIC	homozygous	109090463
20	10373371	10373372	G	C	20	GENIC	homozygous	109090465
20	10375272	10375273	C	A	15	GENIC	homozygous	109090467
20	10377775	10377776	G	A	22	GENIC	homozygous	109237831
20	10365978	10365979	G	C	7	GENIC	homozygous	109463320
20	10365982	10365983	C	A	7	GENIC	homozygous	109463321
20	10379228	10379229	C	T	14	GENIC	homozygous	109237832
20	10379276	10379277	T	C	20	GENIC	homozygous	109237833
20	10379631	10379632	C	T	22	GENIC	homozygous	109237834
20	10379965	10379966	C	T	36	GENIC	homozygous	109237835
20	10381137	10381138	A	G	17	GENIC	homozygous	109237836
20	10381661	10381662	C	T	29	GENIC	homozygous	109237837
20	10383045	10383046	G	A	13	GENIC	homozygous	109237838
20	10384433	10384434	T	A	22	GENIC	homozygous	109237839
20	10384516	10384517	G	A	21	GENIC	homozygous	109237840