chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	119567393	119567393		TGCCCTCGCG	15	GENIC	homozygous	128637506
8	119567395	119567398	TTT		13	GENIC	homozygous	128637507
8	119567402	119567405	TCA		12	GENIC	homozygous	128637508
8	119567406	119567407	A	C	12	GENIC	homozygous	117998054
8	119567408	119567408		CACT	12	GENIC	homozygous	128637509
8	119567412	119567422	TGAATCTTTT		7	GENIC	homozygous	128637510
8	119567425	119567425		CG	7	GENIC	homozygous	128637511
8	119567427	119567427		GCAG	7	GENIC	homozygous	128637512
8	119567428	119567428		GGAC	5	GENIC	homozygous	128637513
8	119567433	119567437	TCTT		2	GENIC	homozygous	128637514
8	119567660	119567661	C	A	2	GENIC	homozygous	117930483
8	119567663	119567664	T	C	2	GENIC	homozygous	117912678
8	119567665	119567665		GAGG	2	GENIC	homozygous	128637515
8	119567667	119567671	TCCT		5	GENIC	homozygous	128637516
8	119571889	119571890	A		15	GENIC	heterozygous	128637520
8	119581700	119581705	AATAA		31	GENIC	homozygous	131054734
8	119628469	119628469		G	42	GENIC	homozygous	128637538
8	119628907	119628908	T	C	13	GENIC	heterozygous	133416550
8	119637539	119637540	T	G	47	GENIC	possibly homozygous	116678266