chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	22865545	22865546	G	A	15	GENIC	homozygous	126007550
4	22865895	22865896	C	T	9	GENIC	homozygous	126007552
4	22867604	22867605	A	G	12	GENIC	homozygous	126007554
4	22869641	22869642	C	A	5	GENIC	homozygous	126007558
4	22869828	22869829	G	A	13	GENIC	homozygous	126007562
4	22869954	22869955	A	G	12	GENIC	homozygous	126007564
4	22870905	22870906	G	T	8	GENIC	homozygous	126007568
4	22870906	22870907	T	A	8	GENIC	homozygous	126007570
4	22871551	22871552	G	T	21	GENIC	homozygous	126007572
4	22872494	22872495	A	G	6	GENIC	homozygous	126007574
4	22876374	22876375	T	G	22	GENIC	homozygous	126007576
4	22878677	22878678	C	T	12	GENIC	homozygous	126007578
4	22879530	22879531	C	T	10	GENIC	homozygous	126007580
4	22880607	22880608	T	C	12	GENIC	homozygous	126007582
4	22880898	22880899	A	G	14	GENIC	homozygous	126007584
4	22883279	22883280	C	T	10	GENIC	homozygous	126007586
4	22885590	22885591	T	G	13	GENIC	homozygous	126007588
4	22886687	22886688	C	A	19	GENIC	homozygous	126007592
4	22887061	22887062	A	G	11	GENIC	homozygous	126007594
4	22889054	22889055	T	G	11	GENIC	homozygous	126007596
4	22889092	22889093	G	A	8	GENIC	homozygous	126007598
4	22889093	22889094	T	G	8	GENIC	homozygous	126007600
4	22889113	22889114	C	G	10	GENIC	homozygous	126007602
4	22889231	22889232	A	G	7	GENIC	homozygous	126007604
4	22889281	22889282	G	A	17	GENIC	homozygous	126007606
4	22889393	22889394	A	G	6	GENIC	homozygous	126007608
4	22890776	22890777	A	C	19	GENIC	homozygous	126007610
4	22890865	22890866	G	C	23	GENIC	possibly homozygous	126007612
4	22890954	22890955	C	T	22	GENIC	possibly homozygous	126007613
4	22884351	22884352	A	G	6	GENIC	homozygous	126047181