chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	11700658	11700659	A	G	45	GENIC	homozygous	109094257
20	11707776	11707777	G	A	31	GENIC	homozygous	109239088
20	11705891	11705892	G	A	15	GENIC	homozygous	109239086
20	11707684	11707685	C	T	31	GENIC	possibly homozygous	109239087
20	11713140	11713141	C	G	32	GENIC	homozygous	109094279
20	11708237	11708238	C	T	30	GENIC	homozygous	109239089
20	11710042	11710043	C	T	23	GENIC	homozygous	109239090
20	11713059	11713060	A	C	29	GENIC	homozygous	109239091
20	11713060	11713061	C	A	30	GENIC	homozygous	109239092
20	11713146	11713147	A	C	33	GENIC	homozygous	109239093
20	11715316	11715317	G	A	25	GENIC	homozygous	109239094
20	11715350	11715351	C	T	21	GENIC	homozygous	109239095
20	11717313	11717314	C	A	22	GENIC	homozygous	109239096
20	11718250	11718251	C	T	38	GENIC	possibly homozygous	109239097
20	11718931	11718932	T	C	24	GENIC	possibly homozygous	109094297
20	11719751	11719752	C	T	31	GENIC	homozygous	109239098
20	11720025	11720026	T	C	13	GENIC	homozygous	109094301
20	11720885	11720886	A	G	23	GENIC	homozygous	109094303