chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	36611366	36611367	T	C	17	GENIC	homozygous	115646943
7	36611889	36611890	C	A	16	GENIC	homozygous	118410979
7	36611910	36611911	A	G	17	GENIC	homozygous	115646944
7	36613865	36613866	C	T	24	GENIC	possibly homozygous	116020757
7	36614866	36614867	T	C	23	GENIC	homozygous	115646950
7	36618947	36618948	C	A	15	GENIC	homozygous	116142761
7	36619448	36619449	A	G	36	GENIC	possibly homozygous	116142763
7	36620640	36620641	G	A	21	GENIC	homozygous	115646959
7	36621408	36621409	A	G	33	GENIC	possibly homozygous	116020767
7	36622360	36622361	G	C	25	GENIC	homozygous	115646961
7	36625275	36625276	T	G	24	GENIC	homozygous	116020773
7	36626370	36626371	G	T	19	GENIC	possibly homozygous	116142775
7	36627460	36627461	T	A	33	GENIC	possibly homozygous	118410980
7	36627575	36627576	G	C	19	GENIC	homozygous	115646968
7	36633119	36633120	G	A	22	GENIC	homozygous	116020783
7	36633409	36633410	C	T	24	GENIC	homozygous	118410981
7	36633832	36633833	T	C	18	GENIC	homozygous	115646979
7	36635669	36635670	G	A	35	GENIC	homozygous	116142783
7	36637346	36637347	T	G	20	GENIC	possibly homozygous	118410982
7	36638184	36638185	C	T	16	GENIC	homozygous	118410983
7	36638712	36638713	A	G	25	GENIC	possibly homozygous	118410984