chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130163269	130163270	G	A	39	GENIC	homozygous	116229419
7	130163689	130163690	A	G	31	GENIC	homozygous	116229420
7	130163737	130163738	T	C	28	GENIC	homozygous	116229421
7	130164645	130164646	G	A	9	GENIC	homozygous	115889432
7	130164914	130164915	G	A	41	GENIC	homozygous	116229422
7	130164959	130164960	C	T	28	GENIC	homozygous	115889434
7	130164972	130164973	G	A	31	GENIC	homozygous	116229423
7	130165072	130165073	A	G	34	GENIC	homozygous	115889436
7	130165668	130165669	C	T	42	GENIC	homozygous	116229424
7	130166033	130166034	G	A	30	GENIC	homozygous	116229425
7	130166106	130166107	T	C	36	GENIC	homozygous	116229426
7	130166140	130166141	C	T	37	GENIC	homozygous	116229427
7	130166631	130166632	A	G	34	GENIC	homozygous	115889440
7	130166792	130166793	C	T	39	GENIC	homozygous	116229428
7	130167383	130167384	T	C	38	GENIC	homozygous	115889442
7	130167588	130167589	T	C	33	GENIC	homozygous	116229429
7	130167907	130167908	C	A	35	GENIC	homozygous	116229430
7	130168071	130168072	T	C	25	GENIC	homozygous	116229431
7	130168523	130168524	A	C	31	GENIC	homozygous	115889446
7	130168639	130168640	C	T	40	GENIC	homozygous	116229432
7	130169146	130169147	C	T	33	GENIC	homozygous	116229433
7	130169395	130169396	G	A	35	GENIC	homozygous	116229434
7	130170720	130170721	C	T	24	GENIC	homozygous	116229435
7	130177396	130177397	T	C	40	GENIC	homozygous	115889466
7	130177548	130177549	C	T	40	GENIC	homozygous	115889468
7	130178013	130178014	A	G	25	GENIC	homozygous	115889470
7	130178243	130178244	T	C	20	GENIC	homozygous	115889474
7	130178249	130178250	T	G	21	GENIC	homozygous	115889476