chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	30902127	30902128	C	A	52	GENIC	possibly homozygous	111523435
3	30902715	30902716	G	A	44	GENIC	possibly homozygous	111523437
3	30906763	30906764	G	A	28	GENIC	homozygous	111523445
3	30906840	30906841	C	T	6	GENIC	homozygous	111901398
3	30906850	30906851	G	C	9	GENIC	homozygous	111901400
3	30907433	30907434	A	G	51	GENIC	possibly homozygous	111523447
3	30907479	30907480	C	T	62	GENIC	possibly homozygous	111523449
3	30910963	30910964	G	T	53	GENIC	homozygous	111523451
3	30912324	30912325	A	G	60	GENIC	homozygous	111523453
3	30912439	30912440	A	G	80	GENIC	homozygous	111523455
3	30912478	30912479	G	A	64	GENIC	homozygous	111523457
3	30912850	30912851	G	C	87	GENIC	homozygous	111523459
3	30913771	30913772	A	G	74	GENIC	homozygous	111523461
3	30913828	30913829	T	C	65	GENIC	homozygous	111523463
3	30913911	30913912	G	C	74	GENIC	homozygous	111523465
3	30915695	30915696	T	C	67	GENIC	homozygous	111523473
3	30913989	30913990	T	C	44	GENIC	homozygous	111523467
3	30914812	30914813	C	G	62	GENIC	homozygous	111523469
3	30915185	30915186	T	C	47	GENIC	possibly homozygous	111523471
3	30916651	30916652	C	G	70	GENIC	homozygous	111523475
3	30917040	30917041	T	C	54	GENIC	homozygous	111523477
3	30917475	30917476	G	A	81	GENIC	homozygous	111523479
3	30917761	30917762	G	A	63	GENIC	homozygous	111523481
3	30917898	30917899	C	T	80	GENIC	homozygous	111523483
3	30918244	30918245	G	T	82	GENIC	homozygous	111523485
3	30919861	30919862	G	T	42	GENIC	homozygous	111523487
3	30920680	30920681	A	C	51	GENIC	possibly homozygous	111523489
3	30921027	30921028	T	C	75	GENIC	homozygous	111523491
3	30921167	30921168	G	C	55	GENIC	homozygous	111523493
3	30923280	30923281	T	C	65	GENIC	homozygous	111901402
3	30926464	30926465	C	T	62	GENIC	homozygous	111523495