chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10672435	10672436	G	A	25	GENIC	possibly homozygous	109422328
20	10672922	10672923	A	G	34	GENIC	possibly homozygous	109422330
20	10673696	10673697	G	T	23	GENIC	homozygous	109422332
20	10675774	10675775	C	T	9	GENIC	homozygous	109422334
20	10676021	10676022	A	G	27	GENIC	homozygous	109090605
20	10676657	10676658	T	C	26	GENIC	heterozygous	109238207
20	10676943	10676944	C	G	31	GENIC	homozygous	109090607
20	10677547	10677548	A	C	10	GENIC	homozygous	109090609
20	10677616	10677617	C	T	23	GENIC	possibly homozygous	109422336
20	10677766	10677767	A	G	24	GENIC	possibly homozygous	109422338
20	10678026	10678027	A	G	14	GENIC	homozygous	109422340
20	10678404	10678405	T	C	40	GENIC	homozygous	109090613
20	10678550	10678551	C	G	29	GENIC	homozygous	109422342
20	10678603	10678604	A	T	15	GENIC	homozygous	109422344
20	10679106	10679107	T	C	10	GENIC	homozygous	109422346