chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130080883	130080884	T	G	30	GENIC	homozygous	54110272
7	130081417	130081418	A	C	27	GENIC	homozygous	54110273
7	130081711	130081719	TTCATGTG	--------	38	GENIC	homozygous	54110274
7	130081826	130081827	A	G	31	GENIC	possibly homozygous	54110275
7	130082062	130082063	T	A	32	GENIC	homozygous	54110276
7	130082104	130082105	G	A	21	GENIC	homozygous	54110277
7	130083749	130083751	GT	--	28	GENIC	homozygous	54110278
7	130084679	130084680	A	AT	22	GENIC	possibly homozygous	54110279
7	130084956	130084957	G	A	28	GENIC	homozygous	54110281
7	130087034	130087035	C	T	34	GENIC	homozygous	54110283
7	130087037	130087038	T	C	30	GENIC	homozygous	54110284
7	130087898	130087899	A	T	35	GENIC	homozygous	54110285
7	130088333	130088334	C	T	23	GENIC	homozygous	54110286
7	130086362	130086363	G	GAA	9	GENIC	heterozygous	55031070
7	130081967	130081968	C	A	28	GENIC	homozygous	54922356