chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	25044308	25044309	A	G	42	GENIC	homozygous	110490938
2	25044578	25044579	C	T	23	GENIC	homozygous	109649079
2	25044931	25044932	G	A	30	GENIC	homozygous	110490940
2	25045335	25045336	A	G	28	GENIC	homozygous	109649085
2	25045450	25045451	T	C	24	GENIC	homozygous	109649087
2	25046312	25046313	C	T	41	GENIC	homozygous	110490942
2	25046618	25046619	A	G	18	GENIC	homozygous	110490944
2	25046810	25046811	C	A	28	GENIC	homozygous	109649095
2	25046934	25046935	T	C	22	GENIC	homozygous	110490946
2	25047127	25047128	C	T	27	GENIC	homozygous	109649098
2	25047146	25047147	A	C	30	GENIC	homozygous	110490948
2	25047154	25047155	T	C	31	GENIC	homozygous	109649100
2	25047184	25047185	C	T	33	GENIC	homozygous	109649102
2	25047268	25047269	C	T	27	GENIC	homozygous	110490950
2	25047573	25047574	T	C	9	GENIC	homozygous	110490952
2	25047835	25047836	C	G	18	GENIC	homozygous	110490954
2	25048048	25048049	C	T	20	GENIC	homozygous	110490956
2	25048152	25048153	C	T	17	GENIC	homozygous	109649110
2	25048338	25048339	G	T	15	GENIC	homozygous	109649112
2	25048397	25048398	A	G	16	GENIC	homozygous	109649114
2	25049245	25049246	A	G	31	GENIC	homozygous	110490958
2	25049282	25049283	A	G	28	GENIC	homozygous	109649116
2	25049364	25049365	A	G	20	GENIC	homozygous	109649118
2	25049843	25049844	C	T	26	GENIC	homozygous	109649122
2	25050929	25050930	A	G	31	GENIC	homozygous	109649130