chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42562652	42562653	A	G	2	GENIC	homozygous	50209360
12	42562974	42562975	G	A	15	GENIC	homozygous	50209361
12	42562978	42562979	C	T	15	GENIC	homozygous	50209362
12	42563266	42563267	G	A	27	GENIC	homozygous	50209364
12	42563331	42563332	T	C	26	GENIC	homozygous	50209365
12	42563763	42563764	A	T	24	GENIC	homozygous	50209366
12	42563999	42564000	A	T	18	GENIC	homozygous	50209367
12	42564116	42564117	A	AAAC	12	GENIC	homozygous	50209368
12	42564129	42564131	AA	--	14	GENIC	possibly homozygous	50209369
12	42564135	42564136	A	C	18	GENIC	possibly homozygous	50544380
12	42564392	42564393	C	CT	2	GENIC	homozygous	50209370
12	42564561	42564562	T	C	30	GENIC	homozygous	50209371
12	42564582	42564583	C	T	25	GENIC	homozygous	50209372
12	42565132	42565133	C	CGATATATATATATATA	5	GENIC	homozygous	50592241
12	42565218	42565219	C	CTTT	5	GENIC	homozygous	50544382
12	42565592	42565593	T	-	19	GENIC	homozygous	50209376
12	42566050	42566051	A	G	26	GENIC	homozygous	50564013
12	42567632	42567633	C	CT	14	GENIC	heterozygous	50327622
12	42567633	42567634	T	-	14	GENIC	heterozygous	50544384
12	42567701	42567702	T	C	13	GENIC	homozygous	50209383
12	42570065	42570068	TAG	---	10	GENIC	homozygous	50383160
12	42570074	42570075	T	C	10	GENIC	homozygous	50383161
12	42572184	42572185	A	AT	12	GENIC	homozygous	50564019
12	42572212	42572214	TT	--	11	GENIC	homozygous	50209389
12	42572440	42572441	A	G	21	GENIC	homozygous	50209390
12	42574591	42574592	C	T	22	GENIC	homozygous	50327632
12	42566239	42566240	T	TTTTATTTA	2	GENIC	homozygous	50804655
12	42576278	42576279	A	G	21	GENIC	homozygous	50804657
12	42572198	42572199	A	AT	11	GENIC	homozygous	50640223