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	6	GENIC	homozygous	50209361
12	42562978	42562979	C	T	6	GENIC	homozygous	50209362
12	42563248	42563249	C	A	13	GENIC	homozygous	50209363
12	42563266	42563267	G	A	14	GENIC	possibly homozygous	50209364
12	42563331	42563332	T	C	16	GENIC	homozygous	50209365
12	42563586	42563588	TC	--	14	GENIC	heterozygous	50599392
12	42563763	42563764	A	T	18	GENIC	homozygous	50209366
12	42563999	42564000	A	T	25	GENIC	homozygous	50209367
12	42564116	42564117	A	AAAC	20	GENIC	homozygous	50209368
12	42564129	42564131	AA	--	19	GENIC	possibly homozygous	50209369
12	42564135	42564136	A	C	21	GENIC	possibly homozygous	50544380
12	42564392	42564393	C	CT	17	GENIC	homozygous	50209370
12	42564561	42564562	T	C	17	GENIC	homozygous	50209371
12	42564582	42564583	C	T	17	GENIC	homozygous	50209372
12	42564639	42564640	C	A	16	GENIC	homozygous	50327620
12	42565170	42565171	G	A	4	GENIC	homozygous	50209374
12	42565218	42565219	C	CTT	1	GENIC	homozygous	50209375
12	42565597	42565603	TTTTTC	------	8	GENIC	homozygous	50209377
12	42566679	42566680	C	A	12	GENIC	homozygous	50209380
12	42566733	42566734	T	C	17	GENIC	homozygous	50209381
12	42567393	42567394	G	T	10	GENIC	homozygous	50209382
12	42567632	42567633	C	CT	8	GENIC	heterozygous	50327622
12	42567633	42567634	T	-	8	GENIC	heterozygous	50544384
12	42567701	42567702	T	C	12	GENIC	homozygous	50209383
12	42567767	42567768	C	G	21	GENIC	homozygous	50209384
12	42568432	42568433	C	A	13	GENIC	homozygous	50209385
12	42568678	42568679	G	A	17	GENIC	homozygous	50209386
12	42569652	42569660	TTTTTTTT	--------	6	GENIC	homozygous	50209387
12	42572185	42572186	T	-	15	GENIC	homozygous	50209388
12	42572213	42572214	T	-	4	GENIC	homozygous	50327624
12	42572440	42572441	A	G	14	GENIC	homozygous	50209390
12	42573679	42573680	T	G	11	GENIC	homozygous	50327626
12	42573975	42573976	T	G	6	GENIC	homozygous	50327628
12	42574404	42574405	C	T	10	GENIC	homozygous	50327630
12	42574591	42574592	C	T	11	GENIC	homozygous	50327632