chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	143952098	143952099	A	C	12	GENIC	homozygous	120148986
2	143952100	143952101	G	C	12	GENIC	homozygous	120148988
2	143952123	143952124	A	G	15	GENIC	homozygous	110038713
2	143952380	143952381	C	T	15	GENIC	homozygous	110761125
2	143952464	143952465	G	T	16	GENIC	homozygous	110761126
2	143952530	143952531	C	T	17	GENIC	homozygous	110761127
2	143955169	143955170	A	T	10	GENIC	homozygous	110761128
2	143957361	143957362	A	G	27	GENIC	homozygous	110761129
2	143957568	143957569	T	G	15	GENIC	homozygous	120148990
2	143957859	143957860	C	T	16	GENIC	homozygous	110761130
2	143957941	143957942	G	A	10	GENIC	homozygous	110761131
2	143960873	143960874	C	T	15	GENIC	homozygous	110038714
2	143960909	143960910	G	A	11	GENIC	homozygous	110038715
2	143961267	143961268	T	C	10	GENIC	homozygous	110038718
2	143962071	143962072	A	C	16	GENIC	homozygous	110038720
2	143962282	143962283	T	C	19	GENIC	homozygous	110038721
2	143963068	143963069	A	G	29	GENIC	homozygous	110038723
2	143964250	143964251	G	A	12	GENIC	homozygous	110761133
2	143964941	143964942	C	G	30	GENIC	homozygous	110038728
2	143965047	143965048	C	T	25	GENIC	homozygous	110761134
2	143965770	143965771	T	C	28	GENIC	homozygous	110038729
2	143966648	143966649	C	A	22	GENIC	homozygous	110761135
2	143967810	143967811	C	T	18	GENIC	homozygous	110038730
2	143967969	143967970	G	A	21	GENIC	homozygous	110761136
2	143968291	143968292	G	C	25	GENIC	homozygous	110761137
2	143968433	143968434	T	C	21	GENIC	homozygous	110038732
2	143969387	143969388	G	A	14	GENIC	homozygous	110761138
2	143969513	143969514	G	T	11	GENIC	homozygous	110761139
2	143969774	143969775	T	C	8	GENIC	homozygous	110038736
2	143971846	143971847	C	T	22	GENIC	homozygous	110761141
2	143971871	143971872	T	C	23	GENIC	homozygous	110038744
2	143974783	143974784	G	A	11	GENIC	homozygous	110761142
2	143977304	143977305	A	C	27	GENIC	homozygous	110038750
2	143977321	143977322	G	A	26	GENIC	homozygous	110038751