chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	61749160	61749161	A	G	27	GENIC	homozygous	116834945
8	61751321	61751322	A	T	24	GENIC	homozygous	116834949
8	61751941	61751942	A	C	35	GENIC	homozygous	116834951
8	61752405	61752406	A	G	16	GENIC	homozygous	116834953
8	61759520	61759521	A	C	12	GENIC	homozygous	117109417
8	61759843	61759844	A	G	14	GENIC	homozygous	116834955
8	61761077	61761078	G	A	23	GENIC	homozygous	117142761
8	61763096	61763097	T	C	11	GENIC	homozygous	116834959
8	61765569	61765570	C	T	24	GENIC	homozygous	116834961
8	61773235	61773236	A	G	22	GENIC	homozygous	116834965
8	61775922	61775923	G	T	21	GENIC	homozygous	116834975
8	61776638	61776639	A	G	17	GENIC	homozygous	117142763
8	61777049	61777050	T	G	24	GENIC	possibly homozygous	116834977
8	61782198	61782199	A	G	19	GENIC	homozygous	116834981
8	61783451	61783452	A	G	8	GENIC	homozygous	116834983
8	61785557	61785558	T	C	31	GENIC	homozygous	116834989
8	61785649	61785650	C	G	23	GENIC	homozygous	117142765
8	61787422	61787423	C	G	18	GENIC	homozygous	116834991
8	61789577	61789578	A	G	22	GENIC	homozygous	116834995
8	61792964	61792965	A	C	11	GENIC	homozygous	117963126
8	61793640	61793641	C	T	15	GENIC	homozygous	116834997
8	61795997	61795998	C	T	15	GENIC	homozygous	116834999
8	61795998	61795999	C	T	15	GENIC	homozygous	116835001
8	61797611	61797612	A	C	24	GENIC	homozygous	116835007
8	61799651	61799652	A	T	18	GENIC	homozygous	116835009
8	61800052	61800053	G	T	19	GENIC	homozygous	116835015
8	61801979	61801980	A	T	23	GENIC	homozygous	116517735
8	61802397	61802398	A	G	11	GENIC	homozygous	117142767