chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10362146	10362147	T	C	30	GENIC	homozygous	109090451
20	10362776	10362777	G	A	29	GENIC	homozygous	109237828
20	10363425	10363426	T	C	24	GENIC	homozygous	109090455
20	10363580	10363581	C	T	31	GENIC	homozygous	109237829
20	10368940	10368941	A	G	23	GENIC	homozygous	109237830
20	10369350	10369351	T	C	14	GENIC	homozygous	109090463
20	10371031	10371032	T	A	7	GENIC	homozygous	109371902
20	10373371	10373372	G	C	19	GENIC	homozygous	109090465
20	10374645	10374646	G	A	22	GENIC	homozygous	109302033
20	10377542	10377543	G	T	11	GENIC	homozygous	109392562
20	10377775	10377776	G	A	28	GENIC	homozygous	109237831
20	10379228	10379229	C	T	28	GENIC	homozygous	109237832
20	10379276	10379277	T	C	39	GENIC	homozygous	109237833
20	10379631	10379632	C	T	30	GENIC	homozygous	109237834
20	10379965	10379966	C	T	39	GENIC	homozygous	109237835
20	10381137	10381138	A	G	28	GENIC	homozygous	109237836
20	10381661	10381662	C	T	24	GENIC	homozygous	109237837
20	10383045	10383046	G	A	27	GENIC	homozygous	109237838
20	10384433	10384434	T	A	27	GENIC	homozygous	109237839
20	10384516	10384517	G	A	29	GENIC	homozygous	109237840
20	10385213	10385214	A	G	32	GENIC	homozygous	109302037