chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	33337565	33337566	C		46	GENIC	homozygous	144914659
12	33337911	33337912	G	A	45	GENIC	homozygous	144923577
12	33337946	33337947	A	G	38	GENIC	homozygous	144923578
12	33338665	33338678	GCAAGTCCCTGCG		39	GENIC	homozygous	144914660
12	33339540	33339541	A	G	45	GENIC	homozygous	139132639
12	33340247	33340248	G	A	52	GENIC	homozygous	144923579
12	33341932	33341933	A		35	GENIC	possibly homozygous	144914661
12	33341935	33341949	AACAACAACACCAA		35	GENIC	possibly homozygous	144914662
12	33342807	33342808	T	C	33	GENIC	homozygous	139132645
12	33343964	33343965	G	A	34	GENIC	homozygous	144923580
12	33344336	33344337	A	G	21	GENIC	homozygous	144923581
12	33345350	33345351	T	C	45	GENIC	homozygous	139132649
12	33345402	33345403	C	A	34	GENIC	homozygous	144923582
12	33348623	33348624	C	A	34	GENIC	homozygous	144923583
12	33349467	33349471	AGAC		32	GENIC	homozygous	144914663
12	33350333	33350334	T		34	GENIC	homozygous	139052884
12	33350465	33350471	TCTGCC		30	GENIC	homozygous	144914664
12	33351582	33351582		T	13	GENIC	homozygous	143523237
12	33351592	33351595	ACA		13	GENIC	homozygous	144914665
12	33351866	33351867	G	A	28	GENIC	homozygous	139132652
12	33351928	33351929	T	C	33	GENIC	homozygous	139132654
12	33352735	33352736	C	A	19	GENIC	homozygous	144923584
12	33353896	33353897	C	T	40	GENIC	homozygous	144923585
12	33356434	33356435	G	A	40	GENIC	homozygous	144923586