chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	70378761	70378762	A	T	38	GENIC	homozygous	115708893
7	70378809	70378810	C	T	40	GENIC	homozygous	115708894
7	70378868	70378869	C	A	52	GENIC	homozygous	115708895
7	70379004	70379005	T	G	40	GENIC	homozygous	115708896
7	70379520	70379521	C	T	32	GENIC	homozygous	115708897
7	70380290	70380291	C	T	37	GENIC	homozygous	115708899
7	70380417	70380418	G	T	33	GENIC	possibly homozygous	115708900
7	70380422	70380423	A	C	33	GENIC	homozygous	115708901
7	70381057	70381058	A	G	40	GENIC	homozygous	115708902
7	70381834	70381835	A	G	26	GENIC	homozygous	115708903
7	70382966	70382967	C	T	24	GENIC	homozygous	115708904
7	70383761	70383762	G	A	27	GENIC	homozygous	115708905
7	70384345	70384346	C	T	46	GENIC	homozygous	115708906
7	70384766	70384767	C	T	37	GENIC	possibly homozygous	115708907
7	70385963	70385964	C	T	44	GENIC	possibly homozygous	115708908
7	70388911	70388912	G	A	34	GENIC	homozygous	115708909
7	70389810	70389811	G	A	37	GENIC	homozygous	115708911
7	70389883	70389884	A	T	43	GENIC	homozygous	115708912
7	70391773	70391774	T	C	20	GENIC	homozygous	115708914
7	70392228	70392229	T	C	33	GENIC	homozygous	115708915
7	70392475	70392476	A	T	35	GENIC	homozygous	115708916
7	70393809	70393810	T	C	47	GENIC	homozygous	116190255
7	70396520	70396521	C	T	35	GENIC	homozygous	115708918
7	70396735	70396736	T	C	38	GENIC	homozygous	115708919
7	70397280	70397281	T	C	33	GENIC	possibly homozygous	115708920
7	70399091	70399092	C	T	43	GENIC	homozygous	115708921
7	70399954	70399955	C	T	38	GENIC	homozygous	115708923
7	70401120	70401121	T	C	44	GENIC	homozygous	115708924
7	70401152	70401153	A	C	50	GENIC	homozygous	115708925
7	70404689	70404690	A	G	34	GENIC	possibly homozygous	116190257
7	70404767	70404768	T	G	34	GENIC	homozygous	116190259