chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48248037	48248038	A	G	48	GENIC	homozygous	115345896
12	48248084	48248085	G	A	43	GENIC	homozygous	115345898
12	48248673	48248674	C	T	55	GENIC	homozygous	115345900
12	48248920	48248921	T	C	53	GENIC	homozygous	115345904
12	48249104	48249105	C	T	61	GENIC	homozygous	115345906
12	48249531	48249532	T	C	25	GENIC	homozygous	115345908
12	48249569	48249570	C	T	23	GENIC	homozygous	115345910
12	48249738	48249739	C	T	42	GENIC	homozygous	115345912
12	48250200	48250201	G	A	46	GENIC	homozygous	115345914
12	48250590	48250591	G	A	44	GENIC	homozygous	115345916
12	48250987	48250988	G	A	39	GENIC	homozygous	115345918
12	48252092	48252093	G	A	23	GENIC	homozygous	115345920
12	48252556	48252557	A	T	46	GENIC	homozygous	115345922
12	48252857	48252858	C	T	47	GENIC	homozygous	115345924
12	48253878	48253879	A	C	5	GENIC	homozygous	115345926
12	48254473	48254474	G	A	21	GENIC	homozygous	115345928
12	48254308	48254308		CTCCCCCA	10	GENIC	heterozygous	128998529
12	48251549	48251549		C	34	GENIC	homozygous	128998527
12	48249061	48249061		GCGCAC	48	GENIC	homozygous	128998526
12	48251561	48251566	AAAAC		34	GENIC	homozygous	128998528
12	48251549	48251550	A	C	33	GENIC	homozygous	129017739
12	48251722	48251723	G	C	45	GENIC	homozygous	115511956
12	48252177	48252178	A	G	12	GENIC	homozygous	115653980