chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	38889650	38889651	C	T	33	GENIC	homozygous	68627063
10	38889791	38889792	A	G	41	GENIC	possibly homozygous	68358751
10	38890186	38890187	A	C	37	GENIC	possibly homozygous	68358753
10	38890228	38890229	C	G	15	GENIC	possibly homozygous	68358755
10	38890332	38890333	C	A	34	GENIC	possibly homozygous	68358757
10	38890679	38890680	T	C	13	GENIC	heterozygous	68358761
10	38890834	38890835	T	C	26	GENIC	possibly homozygous	68358763
10	38890926	38890927	C	T	29	GENIC	heterozygous	68627067
10	38891035	38891036	A	G	33	GENIC	possibly homozygous	68358765
10	38891090	38891091	A	C	21	GENIC	possibly homozygous	68358767
10	38891180	38891181	G	A	29	GENIC	homozygous	68627072
10	38891296	38891297	A	G	25	GENIC	homozygous	68358769
10	38891683	38891684	C	T	17	GENIC	possibly homozygous	68358771
10	38892097	38892098	C	G	17	GENIC	possibly homozygous	68627076
10	38892239	38892240	A	G	23	GENIC	possibly homozygous	68358773
10	38892518	38892519	G	A	16	GENIC	homozygous	68627080