chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	54951656	54951657	T	C	19	GENIC	homozygous	109762925
2	54951724	54951725	C	T	29	GENIC	possibly homozygous	109762927
2	54954319	54954320	T	C	21	GENIC	homozygous	109762933
2	54954997	54954998	A	G	28	GENIC	possibly homozygous	109762935
2	54955053	54955054	T	C	21	GENIC	homozygous	109762937
2	54955606	54955607	T	C	26	GENIC	homozygous	109762938
2	54955811	54955812	A	G	28	GENIC	possibly homozygous	109762942
2	54956208	54956209	C	T	14	GENIC	homozygous	109762946
2	54957507	54957508	A	G	36	GENIC	possibly homozygous	109762948
2	54957992	54957993	A	G	25	GENIC	homozygous	109762950
2	54958116	54958117	G	A	14	GENIC	homozygous	109762952
2	54958378	54958379	G	A	29	GENIC	homozygous	109762954
2	54958544	54958545	G	A	28	GENIC	homozygous	120359096
2	54958835	54958836	A	G	29	GENIC	possibly homozygous	109762956
2	54958896	54958897	A	G	37	GENIC	possibly homozygous	109762958
2	54959171	54959172	C	G	25	GENIC	homozygous	120359097
2	54959319	54959320	G	A	16	GENIC	homozygous	109762960
2	54959865	54959866	T	C	29	GENIC	homozygous	109762962
2	54960374	54960375	T	G	23	GENIC	possibly homozygous	109762964
2	54960397	54960398	C	G	22	GENIC	possibly homozygous	109762966
2	54960422	54960423	G	A	24	GENIC	possibly homozygous	120359098
2	54960944	54960945	T	C	20	GENIC	possibly homozygous	109762968
2	54961481	54961482	T	G	13	GENIC	possibly homozygous	109762970
2	54961817	54961818	T	C	19	GENIC	possibly homozygous	109762972
2	54961859	54961860	G	A	16	GENIC	homozygous	109762974
2	54961961	54961962	A	C	4	GENIC	heterozygous	120359099
2	54962130	54962131	A	T	19	GENIC	possibly homozygous	109762976
2	54962371	54962372	A	G	9	GENIC	heterozygous	109762978
2	54962435	54962436	T	A	9	GENIC	possibly homozygous	109762980
2	54962873	54962874	A	G	26	GENIC	possibly homozygous	109762982
2	54965371	54965372	C	A	19	GENIC	homozygous	109762984