chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	82339319	82339320	G	A	107	GENIC	homozygous	115726981
7	82342284	82342285	T	G	73	GENIC	homozygous	115726982
7	82342805	82342806	T	G	85	GENIC	possibly homozygous	115726983
7	82343934	82343935	A	G	67	GENIC	homozygous	115726984
7	82345459	82345460	A	C	67	GENIC	homozygous	115726985
7	82350245	82350246	T	C	57	GENIC	homozygous	115726986
7	82352630	82352631	G	A	79	GENIC	homozygous	115726987
7	82355377	82355378	T	C	54	GENIC	homozygous	115726988
7	82358997	82358998	G	C	61	GENIC	possibly homozygous	115726989
7	82366087	82366088	G	A	76	GENIC	possibly homozygous	115726990
7	82370473	82370474	A	T	67	GENIC	homozygous	115726991
7	82370513	82370514	G	A	53	GENIC	homozygous	115726992
7	82372466	82372467	G	T	20	GENIC	homozygous	115726994
7	82372597	82372598	T	G	53	GENIC	homozygous	115726995
7	82372696	82372697	T	A	54	GENIC	possibly homozygous	115726996
7	82372759	82372760	A	C	49	GENIC	homozygous	115726997
7	82373189	82373190	G	C	23	GENIC	homozygous	115726998
7	82373857	82373858	G	A	31	GENIC	heterozygous	115726999
7	82373868	82373869	A	T	40	GENIC	heterozygous	115727000
7	82373901	82373902	G	T	39	GENIC	heterozygous	115727001
7	82373945	82373946	T	G	35	GENIC	heterozygous	115727002
7	82374203	82374204	G	C	16	GENIC	heterozygous	115727003
7	82374214	82374215	T	G	14	GENIC	heterozygous	116046621
7	82375125	82375126	C	T	88	GENIC	homozygous	115727005
7	82375131	82375132	T	C	89	GENIC	homozygous	115727006