chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	67808043	67808044	G	A	21	GENIC	possibly homozygous	66325643
13	67808507	67808508	C	T	15	GENIC	homozygous	66325645
13	67808847	67808848	G	A	24	GENIC	homozygous	66325647
13	67809205	67809206	G	T	23	GENIC	homozygous	66325649
13	67809620	67809621	T	C	19	GENIC	possibly homozygous	66076610
13	67809910	67809911	A	G	18	GENIC	homozygous	66076613
13	67812749	67812750	A	T	30	GENIC	possibly homozygous	66325653
13	67813433	67813434	T	C	15	GENIC	homozygous	66325657
13	67813586	67813587	T	C	27	GENIC	homozygous	66076627
13	67814793	67814794	A	G	34	GENIC	homozygous	66325659
13	67815175	67815176	C	T	22	GENIC	homozygous	66325661
13	67816825	67816826	C	T	15	GENIC	possibly homozygous	66325663
13	67818761	67818762	C	G	21	GENIC	homozygous	66076633
13	67819756	67819757	G	A	28	GENIC	possibly homozygous	66325665
13	67820619	67820620	T	C	26	GENIC	homozygous	66325667
13	67822576	67822577	T	C	26	GENIC	homozygous	66076636
13	67822737	67822738	T	C	26	GENIC	homozygous	66076639
13	67822995	67822996	A	G	21	GENIC	homozygous	66076641
13	67823046	67823047	A	C	31	GENIC	possibly homozygous	66076644
13	67823047	67823048	G	T	31	GENIC	homozygous	66076647
13	67826049	67826050	G	A	25	GENIC	homozygous	66076656
13	67826507	67826508	A	G	34	GENIC	homozygous	66076659
13	67828683	67828684	T	C	27	GENIC	homozygous	66076664
13	67829769	67829770	C	A	22	GENIC	possibly homozygous	66076670
13	67830059	67830060	C	T	22	GENIC	possibly homozygous	66076673
13	67831529	67831530	A	G	21	GENIC	homozygous	66076676
13	67832701	67832702	G	T	9	GENIC	homozygous	66076682
13	67828396	67828397	G	A	14	GENIC	heterozygous	67569384