chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106819049	106819050	C	T	54	GENIC	homozygous	117033503
10	106819645	106819646	C	G	52	GENIC	homozygous	116714047
10	106819649	106819650	C	G	51	GENIC	homozygous	116714049
10	106819836	106819837	C	G	43	GENIC	homozygous	117033505
10	106820227	106820228	A	C	45	GENIC	homozygous	116840488
10	106820499	106820500	C	T	35	GENIC	homozygous	116840492
10	106820611	106820612	C	T	47	GENIC	homozygous	117033507
10	106821679	106821680	G	A	39	GENIC	homozygous	117033509
10	106821764	106821765	A	G	35	GENIC	homozygous	116840494
10	106822637	106822638	G	T	50	GENIC	homozygous	117033511
10	106824045	106824046	T	C	49	GENIC	homozygous	116840496
10	106827131	106827132	T	C	46	GENIC	homozygous	116840498
10	106827185	106827186	A	G	54	GENIC	homozygous	116840500
10	106827408	106827409	A	G	49	GENIC	homozygous	116840502
10	106827639	106827640	C	T	48	GENIC	homozygous	117033513
10	106827881	106827882	G	A	45	GENIC	homozygous	116840504
10	106821878	106821880	AG		41	GENIC	homozygous	131471033
10	106828451	106828453	GA		34	GENIC	homozygous	131471035
10	106822153	106822154	C	T	41	GENIC	homozygous	118053113
10	106822199	106822200	T	C	41	GENIC	homozygous	118053114
10	106826187	106826187		TT	43	GENIC	possibly homozygous	131098821