chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	123859285	123859286	C	T	29	GENIC	possibly homozygous	58390441
3	123860959	123860963	CTTA	----	21	GENIC	homozygous	58390442
3	123862108	123862112	ATAT	----	33	GENIC	homozygous	57647524
3	123862113	123862114	T	C	33	GENIC	homozygous	58622189
3	123863801	123863802	G	A	20	GENIC	homozygous	57647530
3	123864040	123864041	A	G	25	GENIC	homozygous	57647532
3	123864445	123864446	T	C	23	GENIC	homozygous	57647534
3	123865031	123865032	G	A	27	GENIC	homozygous	57647536
3	123865817	123865818	G	A	25	GENIC	homozygous	58390443
3	123866758	123866759	G	A	18	GENIC	homozygous	57647538
3	123867093	123867094	A	T	27	GENIC	homozygous	57647540
3	123867277	123867278	G	A	23	GENIC	homozygous	58390444
3	123867646	123867647	A	AGT	7	GENIC	heterozygous	57647542
3	123868012	123868013	G	C	26	GENIC	homozygous	58390445
3	123868837	123868838	G	A	29	GENIC	homozygous	57647548
3	123870006	123870007	A	G	35	GENIC	homozygous	57647552
3	123870098	123870099	G	A	21	GENIC	homozygous	58390446
3	123870275	123870276	G	A	29	GENIC	homozygous	58390447
3	123870895	123870896	T	TAC	22	GENIC	homozygous	57647554
3	123874062	123874063	A	T	19	GENIC	homozygous	58390448
3	123874361	123874362	G	GTA	14	GENIC	homozygous	58390449
3	123874840	123874841	A	C	25	GENIC	possibly homozygous	58390450
3	123875207	123875208	A	AC	17	GENIC	homozygous	57647570
3	123875266	123875267	G	GT	21	GENIC	homozygous	57647572
3	123875570	123875571	A	T	18	GENIC	homozygous	57647574
3	123876038	123876039	A	G	24	GENIC	homozygous	58390451
3	123876314	123876315	C	T	31	GENIC	homozygous	57647578