chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	168051907	168051908	T	C	39	GENIC	homozygous	71525763
5	168052053	168052054	A	G	38	GENIC	homozygous	72472466
5	168052353	168052354	T	C	59	GENIC	homozygous	71201029
5	168052890	168052891	G	A	35	GENIC	homozygous	72472471
5	168053253	168053254	G	A	36	GENIC	homozygous	72472474
5	168053383	168053384	A	G	35	GENIC	homozygous	71201031
5	168053969	168053970	C	T	26	GENIC	possibly homozygous	72472477
5	168054212	168054213	G	A	38	GENIC	homozygous	72472480
5	168054881	168054882	T	G	15	GENIC	homozygous	72472483
5	168055300	168055301	T	C	39	GENIC	homozygous	72472486
5	168057034	168057035	T	C	48	GENIC	homozygous	72472489
5	168057134	168057135	T	C	32	GENIC	homozygous	71201041
5	168057181	168057182	T	C	29	GENIC	homozygous	71201043
5	168057931	168057932	A	T	33	GENIC	homozygous	72472492
5	168058167	168058168	C	T	33	GENIC	homozygous	72472495
5	168058500	168058501	A	T	50	GENIC	homozygous	72472498
5	168058630	168058631	G	A	5	GENIC	homozygous	72472501
5	168058865	168058866	T	C	48	GENIC	homozygous	72472504
5	168059017	168059018	T	A	30	GENIC	homozygous	72472507
5	168059102	168059103	C	T	29	GENIC	homozygous	72472510
5	168059412	168059413	G	A	37	GENIC	homozygous	72472513
5	168059829	168059830	A	G	55	GENIC	homozygous	72472516
5	168060358	168060359	T	C	31	GENIC	homozygous	72472519
5	168061396	168061397	A	T	28	GENIC	homozygous	71525775
5	168061510	168061511	A	G	23	GENIC	homozygous	71201051