chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48803445	48803446	C	T	11	GENIC	homozygous	50491384
12	48803448	48803449	T	G	12	GENIC	homozygous	50491386
12	48803454	48803455	G	A	13	GENIC	homozygous	50491388
12	48803735	48803736	C	CTT	10	GENIC	homozygous	50229490
12	48804690	48804691	G	GC	2	GENIC	homozygous	50229494
12	48805491	48805492	C	T	27	GENIC	homozygous	50229496
12	48805685	48805686	G	GC	25	GENIC	homozygous	50229498
12	48807271	48807272	C	T	24	GENIC	homozygous	50229500
12	48807971	48807972	A	G	29	GENIC	homozygous	50229502
12	48807994	48807995	C	T	31	GENIC	homozygous	50491390
12	48808253	48808254	T	A	30	GENIC	homozygous	50491392
12	48808674	48808678	TGTA	----	6	GENIC	homozygous	50413437
12	48808945	48808946	T	C	15	GENIC	possibly homozygous	50229506
12	48811917	48811918	A	T	12	GENIC	homozygous	50229514
12	48813122	48813123	A	AC	14	GENIC	homozygous	50229520
12	48813275	48813276	C	T	24	GENIC	homozygous	50229522
12	48813584	48813586	AC	--	3	GENIC	homozygous	50503020
12	48814927	48814928	A	AT	15	GENIC	homozygous	50491396
12	48815045	48815050	GGGTC	-----	3	GENIC	homozygous	50229527