chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120648402	120648403	T	G	20	GENIC	homozygous	54084752
7	120648492	120648493	T	C	17	GENIC	homozygous	54084753
7	120649958	120649959	T	C	21	GENIC	homozygous	54084754
7	120649968	120649969	C	CAT	23	GENIC	homozygous	54084755
7	120650260	120650261	T	A	22	GENIC	homozygous	54859856
7	120650286	120650287	G	T	23	GENIC	homozygous	54859857
7	120651078	120651079	C	T	41	GENIC	homozygous	54235030
7	120651265	120651266	G	T	27	GENIC	homozygous	54674619
7	120651766	120651767	G	T	42	GENIC	homozygous	54674621
7	120653103	120653104	A	AGAGTCCG	15	GENIC	homozygous	54235032
7	120653639	120653640	C	T	27	GENIC	homozygous	54674625
7	120654230	120654233	TTT	---	19	GENIC	heterozygous	54235038
7	120654231	120654233	TT	--	19	GENIC	heterozygous	54674627
7	120654445	120654446	T	A	23	GENIC	homozygous	54674629
7	120654711	120654712	C	T	31	GENIC	homozygous	54674631
7	120654718	120654719	G	A	35	GENIC	homozygous	54235042
7	120654723	120654724	G	A	37	GENIC	possibly homozygous	54235044
7	120655086	120655088	AC	--	29	GENIC	homozygous	54674633
7	120655101	120655103	CG	--	33	GENIC	possibly homozygous	54235048
7	120658614	120658615	T	C	34	GENIC	homozygous	54235054
7	120659098	120659099	T	TC	9	GENIC	homozygous	54084757
7	120659475	120659476	G	A	24	GENIC	homozygous	54235064
7	120660796	120660797	G	A	29	GENIC	homozygous	54859858
7	120661585	120661586	C	CG	29	GENIC	homozygous	54235070
7	120662113	120662114	C	T	24	GENIC	homozygous	54859859
7	120662284	120662285	A	G	35	GENIC	homozygous	54859860
7	120664563	120664565	AA	--	7	GENIC	heterozygous	54084758
7	120664860	120664861	T	C	22	GENIC	homozygous	54235074
7	120665160	120665161	G	A	43	GENIC	homozygous	54859861
7	120664562	120664565	AAA	---	7	GENIC	heterozygous	54507792
7	120655601	120655602	A	-	3	GENIC	homozygous	54507790