chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106829688	106829689	T	C	27	GENIC	homozygous	116840508
10	106829788	106829789	T	C	21	GENIC	homozygous	116840510
10	106830348	106830349	C	T	32	GENIC	homozygous	116840514
10	106830983	106830984	G	A	28	GENIC	homozygous	116840518
10	106832135	106832136	C	T	15	GENIC	homozygous	116840526
10	106832874	106832875	C	T	34	GENIC	homozygous	116840528
10	106833486	106833487	A	G	25	GENIC	homozygous	116840530
10	106834834	106834835	C	A	26	GENIC	homozygous	116840532
10	106835689	106835690	A	C	20	GENIC	homozygous	116840536
10	106836055	106836056	C	G	26	GENIC	homozygous	116840538
10	106838790	106838791	T	C	25	GENIC	homozygous	116840540
10	106838904	106838905	A	G	37	GENIC	homozygous	116840542
10	106839125	106839126	T	C	34	GENIC	homozygous	116840544
10	106839424	106839425	G	A	17	GENIC	homozygous	116840546
10	106839580	106839581	C	T	31	GENIC	homozygous	116840548
10	106839879	106839880	T	C	21	GENIC	homozygous	116840550
10	106842883	106842884	G	A	30	GENIC	homozygous	116840558
10	106843205	106843206	G	A	26	GENIC	homozygous	116840560