chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50875218	50875219	C	T	20	GENIC	homozygous	114762508
13	50875945	50875946	G	A	28	GENIC	homozygous	114762510
13	50877180	50877181	G	T	18	GENIC	homozygous	114762512
13	50877502	50877503	C		15	GENIC	homozygous	129052924
13	50878471	50878472	C	T	22	GENIC	homozygous	114762514
13	50879054	50879055	A	G	15	GENIC	homozygous	114762516
13	50879301	50879301		CA	15	GENIC	homozygous	129052925
13	50881299	50881300	C	T	12	GENIC	homozygous	114762518
13	50881582	50881583	T	C	20	GENIC	homozygous	114341831
13	50881792	50881793	A	G	8	GENIC	homozygous	114341835
13	50881812	50881824	CTCTGCACCCAC		8	GENIC	homozygous	129052926
13	50882137	50882138	G	T	24	GENIC	homozygous	114341837
13	50882231	50882232	T	C	20	GENIC	homozygous	114341839
13	50882344	50882345	C	T	16	GENIC	homozygous	114341841
13	50882434	50882435	G	A	23	GENIC	homozygous	114341843
13	50882656	50882657	T	C	10	GENIC	possibly homozygous	114671831
13	50883816	50883823	GGGCTCC		13	GENIC	homozygous	129052928
13	50880718	50880719	T	C	7	GENIC	homozygous	114720356
13	50883094	50883095	A	G	23	GENIC	homozygous	114341845
13	50883783	50883784	G	A	18	GENIC	homozygous	114762520
13	50883798	50883799	A	G	19	GENIC	homozygous	114341847
13	50883831	50883832	G	A	16	GENIC	homozygous	114671833
13	50885057	50885058	C	T	13	GENIC	homozygous	114762522
13	50882989	50882990	G	A	20	GENIC	homozygous	114890293