chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	42562974	42562975	G	A	2	GENIC	homozygous	50209361
12	42562978	42562979	C	T	2	GENIC	homozygous	50209362
12	42563248	42563249	C	A	11	GENIC	possibly homozygous	50209363
12	42563266	42563267	G	A	10	GENIC	homozygous	50209364
12	42563331	42563332	T	C	7	GENIC	homozygous	50209365
12	42563763	42563764	A	T	18	GENIC	homozygous	50209366
12	42563999	42564000	A	T	6	GENIC	homozygous	50209367
12	42564129	42564131	AA	--	4	GENIC	heterozygous	50209369
12	42564135	42564136	A	C	6	GENIC	heterozygous	50544380
12	42564392	42564393	C	CT	19	GENIC	homozygous	50209370
12	42564561	42564562	T	C	8	GENIC	homozygous	50209371
12	42564582	42564583	C	T	6	GENIC	homozygous	50209372
12	42565170	42565171	G	A	3	GENIC	heterozygous	50209374
12	42566679	42566680	C	A	9	GENIC	homozygous	50209380
12	42566733	42566734	T	C	4	GENIC	heterozygous	50209381
12	42567393	42567394	G	T	10	GENIC	homozygous	50209382
12	42567701	42567702	T	C	3	GENIC	heterozygous	50209383
12	42567767	42567768	C	G	7	GENIC	homozygous	50209384
12	42568432	42568433	C	A	11	GENIC	homozygous	50209385
12	42568678	42568679	G	A	16	GENIC	possibly homozygous	50209386
12	42572185	42572186	T	-	2	GENIC	homozygous	50209388
12	42572212	42572214	TT	--	1	GENIC	homozygous	50209389
12	42572440	42572441	A	G	12	GENIC	heterozygous	50209390