chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	25044308	25044309	A	G	15	GENIC	homozygous	110490938
2	25044578	25044579	C	T	13	GENIC	homozygous	109649079
2	25045335	25045336	A	G	10	GENIC	homozygous	109649085
2	25045450	25045451	T	C	8	GENIC	homozygous	109649087
2	25045498	25045499	A	G	13	GENIC	homozygous	109649089
2	25046618	25046619	A	G	15	GENIC	homozygous	110490944
2	25046810	25046811	C	A	21	GENIC	homozygous	109649095
2	25046934	25046935	T	C	17	GENIC	homozygous	110490946
2	25047127	25047128	C	T	10	GENIC	homozygous	109649098
2	25047146	25047147	A	C	5	GENIC	homozygous	110490948
2	25047184	25047185	C	T	9	GENIC	homozygous	109649102
2	25047573	25047574	T	C	6	GENIC	homozygous	110490952
2	25047835	25047836	C	G	11	GENIC	homozygous	110490954
2	25048048	25048049	C	T	28	GENIC	homozygous	110490956
2	25048152	25048153	C	T	15	GENIC	homozygous	109649110
2	25048338	25048339	G	T	22	GENIC	homozygous	109649112
2	25048397	25048398	A	G	12	GENIC	homozygous	109649114
2	25049245	25049246	A	G	17	GENIC	homozygous	110490958
2	25049282	25049283	A	G	20	GENIC	homozygous	109649116
2	25049364	25049365	A	G	16	GENIC	homozygous	109649118
2	25049843	25049844	C	T	18	GENIC	homozygous	109649122