chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	67430990	67430991	C	T	17	GENIC	possibly homozygous	116795555
10	67431887	67431888	A	G	40	GENIC	homozygous	116795557
10	67439698	67439699	T	C	35	GENIC	homozygous	116795559
10	67441625	67441626	T	G	15	GENIC	possibly homozygous	118068219
10	67444240	67444241	C	T	32	GENIC	homozygous	116795561
10	67444347	67444348	G	T	23	GENIC	homozygous	116795563
10	67445423	67445424	C	A	23	GENIC	homozygous	116795565
10	67445547	67445548	G	T	22	GENIC	possibly homozygous	118068220
10	67448696	67448697	A	T	17	GENIC	homozygous	117196363
10	67448732	67448733	A	G	24	GENIC	homozygous	117999143
10	67448701	67448702	C	T	17	GENIC	homozygous	117999140
10	67448718	67448719	A	G	15	GENIC	homozygous	117999141
10	67448720	67448721	T	G	16	GENIC	homozygous	117999142
10	67448741	67448742	A	G	25	GENIC	homozygous	117999144
10	67448753	67448754	T	G	24	GENIC	homozygous	117220559
10	67448762	67448763	C	A	14	GENIC	homozygous	117278298
10	67448763	67448764	T	A	14	GENIC	homozygous	117999145
10	67461006	67461007	A	C	40	GENIC	homozygous	116795567
10	67464502	67464503	G	A	26	GENIC	homozygous	116795569
10	67448768	67448769	T	A	14	GENIC	homozygous	117255963
10	67448770	67448771	C	G	14	GENIC	homozygous	117255965
10	67450926	67450927	T	C	21	GENIC	homozygous	116942555
10	67468334	67468335	T	C	19	GENIC	homozygous	118068221
10	67469756	67469757	G	A	24	GENIC	homozygous	116795571
10	67471282	67471283	A	G	18	GENIC	homozygous	116795573
10	67471587	67471588	A	G	29	GENIC	homozygous	116795575