chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	143952123	143952124	A	G	31	GENIC	homozygous	110038713
2	143960873	143960874	C	T	40	GENIC	homozygous	110038714
2	143960909	143960910	G	A	43	GENIC	homozygous	110038715
2	143961267	143961268	T	C	20	GENIC	homozygous	110038718
2	143961644	143961645	T	G	37	GENIC	homozygous	110038719
2	143962071	143962072	A	C	42	GENIC	homozygous	110038720
2	143962282	143962283	T	C	28	GENIC	homozygous	110038721
2	143962684	143962685	G	A	28	GENIC	homozygous	110038722
2	143963068	143963069	A	G	41	GENIC	homozygous	110038723
2	143963131	143963132	G	T	37	GENIC	homozygous	110038724
2	143964104	143964105	C	T	13	GENIC	homozygous	110038726
2	143964915	143964916	G	A	34	GENIC	homozygous	110038727
2	143964941	143964942	C	G	32	GENIC	homozygous	110038728
2	143965770	143965771	T	C	32	GENIC	homozygous	110038729
2	143967810	143967811	C	T	39	GENIC	homozygous	110038730
2	143968374	143968375	G	A	29	GENIC	homozygous	110038731
2	143968758	143968759	G	A	38	GENIC	homozygous	110038733
2	143969774	143969775	T	C	31	GENIC	homozygous	110038736
2	143971871	143971872	T	C	19	GENIC	homozygous	110038744
2	143973910	143973911	G	A	33	GENIC	homozygous	110038746
2	143977304	143977305	A	C	30	GENIC	homozygous	110038750
2	143977321	143977322	G	A	30	GENIC	homozygous	110038751