chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	82339319	82339320	G	A	58	GENIC	homozygous	115726981
7	82341356	82341357	G	A	38	GENIC	homozygous	116203338
7	82342284	82342285	T	G	43	GENIC	homozygous	115726982
7	82343927	82343928	C	T	45	GENIC	homozygous	116203340
7	82352630	82352631	G	A	68	GENIC	homozygous	115726987
7	82355377	82355378	T	C	38	GENIC	homozygous	115726988
7	82356138	82356139	A	G	25	GENIC	possibly homozygous	116293517
7	82358997	82358998	G	C	62	GENIC	homozygous	115726989
7	82370473	82370474	A	T	39	GENIC	homozygous	115726991
7	82370513	82370514	G	A	44	GENIC	homozygous	115726992
7	82372466	82372467	G	T	32	GENIC	homozygous	115726994
7	82372597	82372598	T	G	56	GENIC	homozygous	115726995
7	82372759	82372760	A	C	45	GENIC	homozygous	115726997
7	82373189	82373190	G	C	18	GENIC	homozygous	115726998
7	82373890	82373891	G	T	18	GENIC	heterozygous	116203342
7	82373901	82373902	G	T	16	GENIC	heterozygous	115727001
7	82373945	82373946	T	G	17	GENIC	heterozygous	115727002
7	82375125	82375126	C	T	55	GENIC	possibly homozygous	115727005
7	82375131	82375132	T	C	51	GENIC	homozygous	115727006
7	82375486	82375487	T	A	51	GENIC	possibly homozygous	116203346
7	82377336	82377337	A	G	47	GENIC	homozygous	116203347