chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5021111	5021112	T	C	24	GENIC	homozygous	109076133
20	5021161	5021162	A	G	21	GENIC	homozygous	109076135
20	5021176	5021177	G	A	22	GENIC	homozygous	109076137
20	5022247	5022248	G	A	30	GENIC	homozygous	109076138
20	5023844	5023845	A	G	25	GENIC	homozygous	109076140
20	5024202	5024203	C	T	7	GENIC	homozygous	109076142
20	5024403	5024404	A	G	20	GENIC	possibly homozygous	109076149
20	5025034	5025035	A	G	17	GENIC	homozygous	109076153
20	5025858	5025859	C	T	23	GENIC	homozygous	109076155
20	5025912	5025913	G	A	25	GENIC	homozygous	109076157
20	5026094	5026095	A	T	15	GENIC	homozygous	109076159
20	5026152	5026153	G	A	3	GENIC	heterozygous	109419940
20	5023516	5023517	C	T	26	GENIC	homozygous	109419934
20	5025119	5025120	T	A	16	GENIC	homozygous	109419936
20	5026148	5026149	G	A	4	GENIC	heterozygous	109419938
20	5026382	5026383	C	T	19	GENIC	homozygous	109076161
20	5026697	5026698	G	C	27	GENIC	homozygous	109076163
20	5027340	5027341	C	T	37	GENIC	possibly homozygous	109076165
20	5027891	5027892	T	C	21	GENIC	homozygous	109076167
20	5028315	5028316	T	C	21	GENIC	homozygous	109076169
20	5028772	5028773	A	C	7	GENIC	homozygous	109419942
20	5028825	5028826	C	T	13	GENIC	homozygous	109076171
20	5029127	5029128	A	T	18	GENIC	homozygous	109419944
20	5029128	5029129	T	G	17	GENIC	homozygous	109419946
20	5029880	5029881	G	A	21	GENIC	homozygous	109419948
20	5029920	5029921	A	G	20	GENIC	homozygous	109296678
20	5030110	5030111	T	C	18	GENIC	homozygous	109296682
20	5030785	5030786	A	G	31	GENIC	homozygous	109296686
20	5030910	5030911	C	T	35	GENIC	homozygous	109419950
20	5031119	5031120	T	A	17	GENIC	homozygous	109419952
20	5031531	5031532	T	C	24	GENIC	homozygous	109419954
20	5031923	5031924	T	C	25	GENIC	homozygous	109076176
20	5032132	5032133	T	C	21	GENIC	homozygous	109076178
20	5033034	5033035	C	T	21	GENIC	homozygous	109076180