chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	108235932	108235933	T	-	31	GENIC	homozygous	51595324
10	108238451	108238452	C	T	64	GENIC	possibly homozygous	51595326
10	108238648	108238649	T	G	51	GENIC	heterozygous	51595328
10	108238663	108238664	G	GTT	22	GENIC	homozygous	51595331
10	108238672	108238673	G	T	40	GENIC	homozygous	51595333
10	108238676	108238677	T	TTTTTTTG	30	GENIC	possibly homozygous	51595335
10	108240909	108240910	A	G	62	GENIC	homozygous	51595337
10	108241604	108241605	T	C	41	GENIC	possibly homozygous	51595339
10	108246885	108246886	A	C	66	GENIC	homozygous	51595343
10	108248059	108248060	C	T	59	GENIC	homozygous	51595345
10	108249366	108249367	A	G	50	GENIC	possibly homozygous	51595347
10	108249539	108249540	C	A	47	GENIC	homozygous	51595350
10	108250641	108250642	C	G	39	GENIC	homozygous	51595352