chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	29868381	29868382	T	C	34	GENIC	homozygous	67838499
10	29868581	29868582	C	T	34	GENIC	homozygous	67838504
10	29870037	29870038	C	T	47	GENIC	homozygous	67838508
10	29870137	29870138	A	G	49	GENIC	homozygous	67838512
10	29870197	29870198	G	A	39	GENIC	homozygous	67838516
10	29870610	29870611	C	T	28	GENIC	homozygous	67838520
10	29870634	29870635	T	C	21	GENIC	homozygous	67838525
10	29870924	29870925	T	C	25	GENIC	possibly homozygous	67838529
10	29870991	29870992	T	C	28	GENIC	homozygous	67838533
10	29871197	29871198	G	T	29	GENIC	homozygous	67838537
10	29874005	29874006	T	C	24	GENIC	heterozygous	67838542
10	29874017	29874018	C	T	18	GENIC	heterozygous	67838546
10	29874167	29874168	A	G	11	GENIC	heterozygous	67838551
10	29874633	29874634	G	T	21	GENIC	homozygous	67838555
10	29875551	29875552	A	T	55	GENIC	possibly homozygous	67838559
10	29875626	29875627	C	T	48	GENIC	homozygous	67838562
10	29875868	29875869	C	T	47	GENIC	homozygous	67838566
10	29876586	29876587	T	C	33	GENIC	homozygous	67838570
10	29876868	29876869	C	T	39	GENIC	homozygous	67838574
10	29878918	29878919	G	A	29	GENIC	homozygous	67838578
10	29880698	29880699	T	C	35	GENIC	homozygous	67838582
10	29880955	29880956	G	A	27	GENIC	homozygous	67838585
10	29882333	29882334	T	A	21	GENIC	heterozygous	67838591