chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	64381454	64381455	A	C	32	GENIC	homozygous	116792361
10	64381574	64381575	C	A	16	GENIC	homozygous	116617330
10	64382843	64382844	T	G	32	GENIC	homozygous	116941643
10	64384235	64384236	T	C	21	GENIC	homozygous	116941645
10	64384266	64384267	A	T	28	GENIC	homozygous	116941647
10	64385796	64385797	A	C	31	GENIC	homozygous	116792365
10	64386321	64386322	A	G	30	GENIC	homozygous	116941649
10	64386519	64386520	G	C	28	GENIC	homozygous	116792367
10	64387554	64387555	T	C	26	GENIC	homozygous	116617334
10	64387860	64387861	T	C	30	GENIC	homozygous	116941651
10	64388325	64388326	A	C	25	GENIC	homozygous	116792371
10	64388784	64388785	A	G	23	GENIC	homozygous	116941653
10	64389404	64389405	C	G	25	GENIC	homozygous	116941655
10	64389873	64389874	A	G	15	GENIC	homozygous	116941657
10	64389912	64389913	T	C	22	GENIC	homozygous	116941659
10	64390042	64390043	T	C	6	GENIC	homozygous	116941661
10	64390047	64390048	T	C	6	GENIC	homozygous	116941663
10	64391569	64391570	C	T	20	GENIC	homozygous	116941665
10	64392255	64392256	T	G	43	GENIC	homozygous	116617338
10	64392364	64392365	G	A	22	GENIC	homozygous	116941667
10	64392580	64392581	G	A	17	GENIC	homozygous	116941669
10	64392609	64392610	A	G	17	GENIC	homozygous	116941671
10	64393549	64393550	T	C	28	GENIC	homozygous	116941673
10	64394398	64394399	C	T	18	GENIC	homozygous	116941675
10	64394779	64394780	T	C	24	GENIC	homozygous	116941677
10	64394990	64394991	C	T	28	GENIC	homozygous	116941679
10	64395734	64395735	T	C	19	GENIC	homozygous	116941681
10	64396111	64396112	T	C	28	GENIC	homozygous	116941683
10	64397763	64397764	G	A	26	GENIC	homozygous	116941685
10	64397894	64397895	C	T	11	GENIC	homozygous	116941687
10	64398245	64398246	A	C	5	GENIC	homozygous	116941689