chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	143952025	143952026	C	T	8	GENIC	homozygous	120206964
2	143952098	143952099	A	C	8	GENIC	homozygous	120148986
2	143952100	143952101	G	C	9	GENIC	homozygous	120148988
2	143952123	143952124	A	G	9	GENIC	homozygous	110038713
2	143953362	143953363	G	A	25	GENIC	homozygous	120206965
2	143954119	143954120	C	T	25	GENIC	homozygous	120206966
2	143955169	143955170	A	T	16	GENIC	homozygous	110761128
2	143957361	143957362	A	G	15	GENIC	homozygous	110761129
2	143957568	143957569	T	G	14	GENIC	homozygous	120148990
2	143960873	143960874	C	T	9	GENIC	homozygous	110038714
2	143961267	143961268	T	C	11	GENIC	homozygous	110038718
2	143961897	143961898	C	T	28	GENIC	homozygous	120206967
2	143961948	143961949	T	C	33	GENIC	homozygous	120206968
2	143962071	143962072	A	C	23	GENIC	homozygous	110038720
2	143962208	143962209	G	A	27	GENIC	homozygous	120206969
2	143962282	143962283	T	C	38	GENIC	homozygous	110038721
2	143962734	143962735	G	C	22	GENIC	homozygous	120206970
2	143962856	143962857	G	A	10	GENIC	homozygous	120206971
2	143963068	143963069	A	G	22	GENIC	homozygous	110038723
2	143963131	143963132	G	T	22	GENIC	homozygous	110038724
2	143964207	143964208	G	A	25	GENIC	homozygous	120206972
2	143964941	143964942	C	G	17	GENIC	homozygous	110038728
2	143965770	143965771	T	C	28	GENIC	homozygous	110038729
2	143966130	143966131	T	G	20	GENIC	homozygous	120206973
2	143966982	143966983	C	A	22	GENIC	homozygous	120206974
2	143968433	143968434	T	C	21	GENIC	homozygous	110038732
2	143969774	143969775	T	C	13	GENIC	homozygous	110038736
2	143971871	143971872	T	C	25	GENIC	homozygous	110038744
2	143961090	143961091	G	C	18	GENIC	homozygous	120372753
2	143977304	143977305	A	C	19	GENIC	homozygous	110038750
2	143977321	143977322	G	A	22	GENIC	homozygous	110038751