chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5021111	5021112	T	C	12	GENIC	homozygous	109076133
20	5021161	5021162	A	G	12	GENIC	homozygous	109076135
20	5021176	5021177	G	A	14	GENIC	homozygous	109076137
20	5022247	5022248	G	A	13	GENIC	homozygous	109076138
20	5023844	5023845	A	G	10	GENIC	homozygous	109076140
20	5024202	5024203	C	T	6	GENIC	homozygous	109076142
20	5024403	5024404	A	G	9	GENIC	homozygous	109076149
20	5025034	5025035	A	G	26	GENIC	homozygous	109076153
20	5025858	5025859	C	T	13	GENIC	homozygous	109076155
20	5025912	5025913	G	A	22	GENIC	homozygous	109076157
20	5026094	5026095	A	T	26	GENIC	homozygous	109076159
20	5026382	5026383	C	T	13	GENIC	homozygous	109076161
20	5026697	5026698	G	C	22	GENIC	homozygous	109076163
20	5027340	5027341	C	T	22	GENIC	homozygous	109076165
20	5027891	5027892	T	C	26	GENIC	homozygous	109076167
20	5028315	5028316	T	C	16	GENIC	homozygous	109076169
20	5029920	5029921	A	G	14	GENIC	homozygous	109296678
20	5030110	5030111	T	C	22	GENIC	homozygous	109296682
20	5030116	5030117	A	C	20	GENIC	homozygous	109296684
20	5030785	5030786	A	G	15	GENIC	homozygous	109296686
20	5030909	5030910	G	T	27	GENIC	homozygous	109390145
20	5031374	5031375	T	C	21	GENIC	homozygous	109390146
20	5032592	5032593	G	A	30	GENIC	homozygous	109390147
20	5032612	5032613	C	T	31	GENIC	homozygous	109390148
20	5034930	5034931	T	G	19	GENIC	homozygous	109390149