chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	70362579	70362580	T	C	50	GENIC	homozygous	53956258
7	70362801	70362802	T	C	40	GENIC	homozygous	53956259
7	70363002	70363003	A	-	44	GENIC	homozygous	54444868
7	70363465	70363466	G	T	47	GENIC	possibly homozygous	53956261
7	70364808	70364810	GT	--	6	GENIC	homozygous	53956270
7	70366624	70366625	C	T	35	GENIC	homozygous	53956287
7	70367293	70367294	C	A	50	GENIC	homozygous	54444870
7	70367790	70367791	G	C	7	GENIC	possibly homozygous	53956306
7	70369108	70369109	T	C	55	GENIC	homozygous	53956310
7	70369647	70369648	A	G	56	GENIC	homozygous	53956313
7	70369785	70369786	C	A	21	GENIC	homozygous	54444874
7	70369789	70369790	C	A	22	GENIC	homozygous	54444876
7	70369793	70369794	C	A	22	GENIC	possibly homozygous	54444878
7	70369928	70369929	A	-	33	GENIC	possibly homozygous	53956315
7	70367396	70367397	A	ATT	24	GENIC	homozygous	54656818
7	70371005	70371006	A	AGGACGGAC	9	GENIC	homozygous	54444880
7	70371316	70371317	C	T	43	GENIC	possibly homozygous	54444882
7	70372983	70372984	T	C	48	GENIC	homozygous	54444884
7	70373441	70373442	T	C	38	GENIC	possibly homozygous	54444886
7	70373610	70373611	T	C	32	GENIC	possibly homozygous	53956336
7	70373624	70373625	T	C	34	GENIC	homozygous	53956338
7	70373831	70373832	T	C	50	GENIC	homozygous	54444889
7	70374003	70374004	G	-	38	GENIC	homozygous	54444891
7	70374659	70374665	ATAAAT	------	19	GENIC	homozygous	54444893
7	70374677	70374681	CTTT	----	29	GENIC	heterozygous	54444895
7	70374995	70374998	TTT	---	24	GENIC	possibly homozygous	54444897
7	70375149	70375150	G	A	39	GENIC	homozygous	54444899
7	70375596	70375597	A	G	36	GENIC	homozygous	54444902
7	70375951	70375952	A	G	14	INTERGENIC	homozygous	54444904
7	70376402	70376403	T	-	38	INTERGENIC	heterozygous	54444906
7	70376530	70376531	G	A	62	INTERGENIC	homozygous	54444908
7	70376987	70376988	A	G	47	INTERGENIC	homozygous	54444910