chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	38889650	38889651	C	T	36	GENIC	possibly homozygous	68627063
10	38889791	38889792	A	G	59	GENIC	homozygous	68358751
10	38890186	38890187	A	C	44	GENIC	homozygous	68358753
10	38890228	38890229	C	G	47	GENIC	homozygous	68358755
10	38890332	38890333	C	A	39	GENIC	homozygous	68358757
10	38890578	38890579	C	T	11	GENIC	homozygous	69032750
10	38890679	38890680	T	C	40	GENIC	homozygous	68358761
10	38890834	38890835	T	C	3	GENIC	homozygous	68358763
10	38891035	38891036	A	G	19	GENIC	homozygous	68358765
10	38891090	38891091	A	C	18	GENIC	homozygous	68358767
10	38891180	38891181	G	A	21	GENIC	homozygous	68627072
10	38891296	38891297	A	G	41	GENIC	homozygous	68358769
10	38891683	38891684	C	T	13	GENIC	homozygous	68358771
10	38892097	38892098	C	G	10	GENIC	homozygous	68627076
10	38892239	38892240	A	G	49	GENIC	homozygous	68358773
10	38892518	38892519	G	A	38	GENIC	homozygous	68627080