chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	50951267	50951268	G	T	18	GENIC	homozygous	111565381
3	50951270	50951270		G	18	GENIC	homozygous	127880396
3	50951273	50951273		T	17	GENIC	homozygous	127880397
3	50951277	50951278	G		17	GENIC	homozygous	127880398
3	50951308	50951308		A	20	GENIC	homozygous	127880399
3	50951348	50951348		C	19	GENIC	homozygous	127880400
3	50951452	50951452		C	26	GENIC	homozygous	127880401
3	50964995	50964995		AG	11	GENIC	homozygous	127880412
3	50965078	50965078		A	21	GENIC	homozygous	127880413
3	50965094	50965095	G	T	22	GENIC	homozygous	119649168
3	50965095	50965096	T	A	22	GENIC	homozygous	111906211
3	50965116	50965116		C	25	GENIC	homozygous	127880414
3	50965163	50965164	G	A	23	GENIC	homozygous	111565431
3	50978527	50978528	A		4	GENIC	homozygous	127880420
3	50978530	50978530		G	4	GENIC	homozygous	127880421
3	50978537	50978537		G	4	GENIC	homozygous	127880422
3	50978538	50978539	T	G	4	GENIC	homozygous	119828683
3	50965005	50965006	A		11	GENIC	homozygous	130540870
3	50979653	50979654	C	A	12	GENIC	heterozygous	130543427
3	50979654	50979655	T	G	12	GENIC	heterozygous	130543428
3	51004896	51004897	A	T	5	GENIC	heterozygous	130543429
3	51042775	51042776	A		4	GENIC	homozygous	130540871