chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130752159	130752160	A	G	37	GENIC	homozygous	138224564
7	130752616	130752617	C	G	27	GENIC	homozygous	138224565
7	130752630	130752631	C	G	30	GENIC	homozygous	138224566
7	130752738	130752739	C	G	44	GENIC	homozygous	138224567
7	130752742	130752743	G	C	45	GENIC	homozygous	138224568
7	130752744	130752745	G	C	44	GENIC	homozygous	138224569
7	130752830	130752831	G	C	55	GENIC	homozygous	138224570
7	130753817	130753818	T	C	52	GENIC	homozygous	138224571
7	130758252	130758253	A	C	39	GENIC	homozygous	138224572
7	130759105	130759105		GT	45	GENIC	possibly homozygous	137983934
7	130759632	130759633	A		47	GENIC	homozygous	137983935
7	130760584	130760588	AGAC		34	GENIC	homozygous	137983936
7	130760903	130760904	A	G	42	GENIC	homozygous	138224573
7	130765118	130765118		T	41	GENIC	possibly homozygous	137983937
7	130766091	130766091		A	39	GENIC	possibly homozygous	137983938
7	130766706	130766713	GTGAAGA		44	GENIC	homozygous	137983939
7	130767004	130767005	T	C	55	GENIC	homozygous	138224574
7	130767180	130767181	A	G	60	GENIC	possibly homozygous	138224575
7	130768369	130768371	CT		62	GENIC	homozygous	137983940
7	130768387	130768388	T	A	59	GENIC	homozygous	138224576
7	130768485	130768486	C	T	49	GENIC	homozygous	138224577
7	130770744	130770744		A	30	GENIC	possibly homozygous	137983941
7	130771057	130771058	C	A	59	GENIC	homozygous	138224578
7	130771067	130771068	T	G	58	GENIC	homozygous	138224579
7	130772364	130772365	A	C	12	GENIC	possibly homozygous	138224580
7	130772841	130772842	G	A	54	GENIC	homozygous	138224581
7	130777068	130777069	C	T	64	GENIC	homozygous	138224582
7	130777845	130777846	A	G	62	GENIC	homozygous	138224583
7	130779824	130779825	C	G	15	GENIC	homozygous	144388468
7	130779828	130779829	C	G	16	GENIC	homozygous	144388469