chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	56884211	56884212	C	T	17	GENIC	homozygous	109767725
2	56884229	56884230	A	G	18	GENIC	homozygous	109767727
2	56886075	56886076	T	G	22	GENIC	homozygous	109767729
2	56886454	56886455	G	C	19	GENIC	homozygous	109767731
2	56886516	56886517	G	A	16	GENIC	homozygous	109767733
2	56886614	56886615	T	C	25	GENIC	homozygous	109767735
2	56886653	56886654	C	G	25	GENIC	homozygous	109767737
2	56887412	56887413	T	C	6	GENIC	homozygous	109767739
2	56888058	56888059	G	C	13	GENIC	homozygous	109767741
2	56888069	56888070	A	T	14	GENIC	homozygous	109767743
2	56888905	56888906	A	G	12	GENIC	homozygous	109767745
2	56889551	56889552	A	C	17	GENIC	homozygous	109767747
2	56890022	56890023	T	C	19	GENIC	homozygous	109767749
2	56890860	56890861	G	C	9	GENIC	homozygous	109767750
2	56892579	56892580	C	G	15	GENIC	homozygous	109767752
2	56893140	56893141	A	C	30	GENIC	homozygous	109767754
2	56893145	56893146	C	T	28	GENIC	homozygous	109767756
2	56893860	56893861	A	G	21	GENIC	homozygous	109767758
2	56890155	56890156	T	A	11	GENIC	homozygous	120124156
2	56890157	56890158	T	A	11	GENIC	homozygous	120124157
2	56902694	56902695	G	A	17	GENIC	homozygous	109767762
2	56903577	56903578	G	C	21	GENIC	homozygous	109767764