chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106819049	106819050	C	T	19	GENIC	homozygous	117033503
10	106819645	106819646	C	G	19	GENIC	homozygous	116714047
10	106819649	106819650	C	G	19	GENIC	homozygous	116714049
10	106819836	106819837	C	G	15	GENIC	homozygous	117033505
10	106820227	106820228	A	C	27	GENIC	homozygous	116840488
10	106820499	106820500	C	T	34	GENIC	homozygous	116840492
10	106820611	106820612	C	T	21	GENIC	homozygous	117033507
10	106821679	106821680	G	A	23	GENIC	homozygous	117033509
10	106821764	106821765	A	G	29	GENIC	homozygous	116840494
10	106822637	106822638	G	T	19	GENIC	homozygous	117033511
10	106824045	106824046	T	C	10	GENIC	homozygous	116840496
10	106827131	106827132	T	C	22	GENIC	homozygous	116840498
10	106827185	106827186	A	G	17	GENIC	homozygous	116840500
10	106827408	106827409	A	G	25	GENIC	homozygous	116840502
10	106827639	106827640	C	T	16	GENIC	homozygous	117033513
10	106827881	106827882	G	A	18	GENIC	homozygous	116840504