chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	14311702	14311703	C	T	20	GENIC	homozygous	119329487
17	14312139	14312140	G	C	60	GENIC	homozygous	111335998
17	14312218	14312219	T	G	50	GENIC	homozygous	119329488
17	14312220	14312221	A	C	48	GENIC	possibly homozygous	119329489
17	14312221	14312222	T	C	48	GENIC	homozygous	119329490
17	14312288	14312289	C	T	61	GENIC	homozygous	119329491
17	14312301	14312302	T	C	55	GENIC	possibly homozygous	119329492
17	14312483	14312484	C	T	38	GENIC	homozygous	119329493
17	14317933	14317934	G	A	54	GENIC	heterozygous	119329494
17	14319658	14319659	G	T	124	GENIC	heterozygous	119329495
17	14319732	14319733	G	A	125	GENIC	heterozygous	119265913
17	14319734	14319735	G	A	126	GENIC	heterozygous	119329496
17	14319797	14319798	T	C	112	GENIC	possibly homozygous	111336002
17	14319803	14319804	G	C	108	GENIC	heterozygous	119329497
17	14319855	14319856	T	C	86	GENIC	heterozygous	111336004
17	14319948	14319949	G	T	69	GENIC	heterozygous	119265914
17	14319985	14319986	A	G	54	GENIC	heterozygous	119265916