chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	143893156	143893157	G	C	18	GENIC	homozygous	110038643
2	143897498	143897499	G	A	33	GENIC	homozygous	110761082
2	143900941	143900942	C	T	18	GENIC	homozygous	110761083
2	143902757	143902758	T	C	13	GENIC	homozygous	110761084
2	143904679	143904680	G	A	10	GENIC	homozygous	110761085
2	143904961	143904962	C	T	11	GENIC	homozygous	110761086
2	143905700	143905701	A	G	22	GENIC	homozygous	110038655
2	143908649	143908650	C	T	27	GENIC	homozygous	110761087
2	143909624	143909625	A	G	25	GENIC	homozygous	110038662
2	143910190	143910191	A	C	20	GENIC	homozygous	110038664
2	143910525	143910526	T	A	20	GENIC	homozygous	110761088
2	143910940	143910941	A	G	17	GENIC	homozygous	110761089
2	143912117	143912118	A	G	24	GENIC	homozygous	110038666
2	143914519	143914520	A	G	19	GENIC	homozygous	110761090
2	143914528	143914529	T	C	16	GENIC	homozygous	110038668
2	143915327	143915328	A	T	12	GENIC	homozygous	110761091
2	143916086	143916087	C	A	28	GENIC	homozygous	110038669
2	143917310	143917311	G	A	17	GENIC	homozygous	110761092
2	143918369	143918370	C	T	8	GENIC	homozygous	110761094
2	143921988	143921989	G	A	18	GENIC	homozygous	110761095
2	143923832	143923833	C	T	18	GENIC	homozygous	110038678
2	143923868	143923869	T	A	19	GENIC	homozygous	110038679
2	143925217	143925218	T	C	21	GENIC	homozygous	110761096