chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	78496686	78496687	G	T	20	GENIC	possibly homozygous	113125652
4	78497985	78497986	C		19	GENIC	homozygous	130933116
4	78499025	78499026	T	C	17	GENIC	homozygous	112738435
4	78501065	78501066	T	A	17	GENIC	homozygous	112738443
4	78502373	78502374	T	C	21	GENIC	homozygous	112738455
4	78502649	78502670	CCTAAAAGTAACTTTATCTGG		27	GENIC	homozygous	130933117
4	78503798	78503799	A	G	24	GENIC	homozygous	112738466
4	78504207	78504208	T	A	20	GENIC	homozygous	113125653
4	78504560	78504561	A	G	23	GENIC	homozygous	112738468
4	78505026	78505027	G	A	23	GENIC	homozygous	113125654
4	78505293	78505294	G	A	13	GENIC	homozygous	112738472
4	78506924	78506925	C	T	29	GENIC	homozygous	113125655
4	78507556	78507557	G	T	19	GENIC	homozygous	112738476
4	78508911	78508911		GT	24	GENIC	homozygous	130933118
4	78509279	78509280	G	C	22	GENIC	homozygous	112738480
4	78510693	78510694	G	A	18	GENIC	homozygous	112738486
4	78511216	78511217	T	C	19	GENIC	homozygous	113352368
4	78511718	78511719	C	T	25	GENIC	homozygous	113352370
4	78512347	78512348	T	G	19	GENIC	homozygous	112738488
4	78504471	78504472	G	A	10	GENIC	homozygous	113459009
4	78509033	78509034	T	C	20	GENIC	homozygous	113459011
4	78513456	78513457	A	C	17	GENIC	homozygous	112738492
4	78513827	78513828	G	T	20	GENIC	homozygous	112738494
4	78514281	78514282	T	C	21	GENIC	homozygous	112738496