chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	11700658	11700659	A	G	42	GENIC	homozygous	109094257
20	11705557	11705558	T	C	15	GENIC	homozygous	109302363
20	11705891	11705892	G	A	28	GENIC	homozygous	109239086
20	11707684	11707685	C	T	42	GENIC	homozygous	109239087
20	11707776	11707777	G	A	30	GENIC	homozygous	109239088
20	11708237	11708238	C	T	29	GENIC	homozygous	109239089
20	11710042	11710043	C	T	34	GENIC	homozygous	109239090
20	11713059	11713060	A	C	42	GENIC	possibly homozygous	109239091
20	11713140	11713141	C	G	27	GENIC	homozygous	109094279
20	11713146	11713147	A	C	28	GENIC	possibly homozygous	109239093
20	11715316	11715317	G	A	34	GENIC	homozygous	109239094
20	11715350	11715351	C	T	38	GENIC	homozygous	109239095
20	11717313	11717314	C	A	39	GENIC	homozygous	109239096
20	11718250	11718251	C	T	39	GENIC	homozygous	109239097
20	11718931	11718932	T	C	41	GENIC	homozygous	109094297
20	11719751	11719752	C	T	39	GENIC	homozygous	109239098
20	11720025	11720026	T	C	36	GENIC	homozygous	109094301
20	11720885	11720886	A	G	35	GENIC	homozygous	109094303