chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	14059627	14059628	C	T	45	GENIC	possibly homozygous	140059220
17	14063001	14063001		AACC	14	GENIC	possibly homozygous	140010391
17	14063637	14063638	A	C	11	GENIC	possibly homozygous	140059221
17	14064135	14064136	T	A	34	GENIC	homozygous	140059222
17	14065927	14065928	A	G	37	GENIC	homozygous	140059223
17	14066147	14066148	G	A	24	GENIC	homozygous	140059224
17	14068339	14068340	T	G	40	GENIC	homozygous	140059225
17	14069834	14069834		GAGAGGGAGGGA	13	GENIC	homozygous	140010392
17	14072131	14072132	A	G	47	GENIC	homozygous	140059226
17	14073562	14073563	G	A	33	GENIC	homozygous	140059227
17	14078449	14078450	C	A	46	GENIC	possibly homozygous	140059228
17	14080243	14080243		CGCACG	18	GENIC	possibly homozygous	140010393
17	14084576	14084577	G	A	45	GENIC	homozygous	140059229
17	14084891	14084892	C	T	42	GENIC	homozygous	140059230
17	14091389	14091414	AGATAAAGGATGAGTCCCCTGCGAT		32	GENIC	homozygous	140010394
17	14093859	14093860	A	C	40	GENIC	possibly homozygous	140059231
17	14096137	14096138	A	G	45	GENIC	homozygous	140059232
17	14099661	14099668	AGTCTCA		14	GENIC	homozygous	140010395