chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22139012	22139013	G	A	23	GENIC	homozygous	115280457
12	22139019	22139020	A	T	24	GENIC	homozygous	115280459
12	22139443	22139444	T	C	27	GENIC	homozygous	115280461
12	22139487	22139488	T	C	35	GENIC	homozygous	115280463
12	22139493	22139494	A	G	33	GENIC	homozygous	115280465
12	22139501	22139502	G	T	37	GENIC	homozygous	115280467
12	22139649	22139650	T	A	20	GENIC	homozygous	115280469
12	22139931	22139932	C	T	36	GENIC	possibly homozygous	115280473
12	22140656	22140657	T	C	35	GENIC	homozygous	115280477
12	22141508	22141509	C	T	24	GENIC	homozygous	115280479
12	22141964	22141965	T	G	22	GENIC	homozygous	115280481
12	22141986	22141987	A	G	26	GENIC	homozygous	115280483
12	22142874	22142875	T	C	22	GENIC	homozygous	115280485
12	22143718	22143719	T	A	43	GENIC	possibly homozygous	115366472
12	22143721	22143722	C	T	39	GENIC	possibly homozygous	115280487
12	22144612	22144613	T	C	30	GENIC	homozygous	115280491
12	22145026	22145027	T	A	27	GENIC	homozygous	115280495
12	22145332	22145333	T	A	39	GENIC	homozygous	115366474
12	22146395	22146396	C	T	47	GENIC	homozygous	115280499
12	22143654	22143655	C	A	35	GENIC	possibly homozygous	115469479
12	22148009	22148010	A	G	35	GENIC	homozygous	115280505
12	22148198	22148199	T	A	27	GENIC	homozygous	115280507
12	22148439	22148440	A	G	44	GENIC	homozygous	115280509
12	22148973	22148974	C	T	30	GENIC	homozygous	115280513
12	22149312	22149313	G	C	37	GENIC	homozygous	115280515
12	22149839	22149840	G	A	50	GENIC	possibly homozygous	115280517
12	22150042	22150043	C	T	47	GENIC	possibly homozygous	115366476
12	22150159	22150160	C	T	35	GENIC	possibly homozygous	115280519
12	22150331	22150332	A	G	34	GENIC	homozygous	115280521
12	22150372	22150373	A	G	42	GENIC	homozygous	115280523
12	22150628	22150629	G	A	33	GENIC	homozygous	115280525
12	22151576	22151577	T	C	20	GENIC	homozygous	115280527
12	22152027	22152028	T	C	43	GENIC	homozygous	115280529
12	22153142	22153143	G	A	37	GENIC	homozygous	115280533