chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	141163610	141163611	A	G	32	GENIC	homozygous	54157861
7	141164637	141164638	A	G	29	GENIC	homozygous	54157862
7	141164750	141164751	G	A	43	GENIC	homozygous	54157863
7	141164823	141164824	A	T	34	GENIC	homozygous	54157864
7	141165014	141165015	G	A	24	GENIC	homozygous	54157866
7	141165110	141165111	G	A	31	GENIC	homozygous	54157868
7	141165795	141165796	A	T	18	GENIC	homozygous	54157869
7	141166252	141166253	T	C	23	GENIC	homozygous	54157870
7	141166355	141166356	C	T	23	GENIC	homozygous	54157871
7	141166814	141166815	T	A	30	GENIC	homozygous	54157872
7	141167190	141167191	G	A	29	GENIC	homozygous	54157873
7	141167880	141167881	T	C	26	GENIC	homozygous	54157875
7	141168416	141168417	C	CAA	11	GENIC	heterozygous	55032224
7	141168660	141168661	A	C	19	GENIC	homozygous	54157876
7	141165742	141165743	A	AACACACACACAC	17	GENIC	possibly homozygous	55363386
7	141165742	141165743	A	AACACACACAC	17	GENIC	heterozygous	55768357
7	141165859	141165860	G	GCACACACACA	13	GENIC	homozygous	55735471
7	141168416	141168417	C	CA	11	GENIC	heterozygous	54265152
7	141166343	141166344	C	A	24	GENIC	homozygous	55680243
7	141167340	141167341	G	A	28	GENIC	homozygous	55680245
7	141168112	141168113	G	A	38	GENIC	homozygous	55680247