chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39997994	39997995	C	G	59	GENIC	homozygous	116801777
8	39999046	39999047	C	T	61	GENIC	homozygous	116801779
8	39999106	39999107	A	G	59	GENIC	homozygous	116801781
8	39999341	39999342	G	T	65	GENIC	possibly homozygous	116801783
8	39999397	39999398	T	G	59	GENIC	homozygous	116801785
8	39999423	39999424	C	T	63	GENIC	homozygous	116801787
8	40000157	40000158	C	T	44	GENIC	homozygous	116801789
8	40000333	40000334	A	G	54	GENIC	homozygous	116801791
8	40000400	40000401	G	A	52	GENIC	homozygous	116801793
8	40001913	40001914	A	G	70	GENIC	homozygous	116463666
8	40002014	40002015	A	G	57	GENIC	homozygous	116463667
8	40002067	40002068	A	G	50	GENIC	homozygous	116801795
8	40002403	40002404	T	C	56	GENIC	heterozygous	116463669
8	40003385	40003386	C	G	50	GENIC	homozygous	116801797
8	40003399	40003400	G	C	58	GENIC	homozygous	116463677
8	40003427	40003428	G	A	59	GENIC	possibly homozygous	116801799
8	40003876	40003877	T	C	34	GENIC	homozygous	116801801
8	40005382	40005383	C	T	16	GENIC	heterozygous	116463684
8	40005492	40005493	G	A	36	GENIC	possibly homozygous	116801803
8	40005498	40005499	A	G	40	GENIC	heterozygous	116801805
8	40008616	40008617	C	T	54	GENIC	possibly homozygous	116801807