chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	82068847	82068848	T	G	25	GENIC	possibly homozygous	116845015
8	82074300	82074301	A	G	67	GENIC	heterozygous	116530395
8	82074322	82074323	G	A	71	GENIC	heterozygous	128662168
8	82074323	82074324	G	A	71	GENIC	heterozygous	128662169
8	82074324	82074325	G	C	69	GENIC	heterozygous	128662170
8	82074338	82074339	G	A	63	GENIC	heterozygous	117048503
8	82074348	82074360	CAAGGCTCCACC		64	GENIC	heterozygous	131445213
8	82084667	82084668	T	A	25	GENIC	homozygous	116530417
8	82084685	82084685		A	30	GENIC	homozygous	128606814
8	82084732	82084732		TAACTG	34	GENIC	homozygous	128606815
8	82097038	82097039	C	G	13	GENIC	heterozygous	132324619
8	82133459	82133460	A	T	27	GENIC	homozygous	116845020
8	82133460	82133461	A	T	27	GENIC	homozygous	116845021
8	82133461	82133462	A	G	27	GENIC	homozygous	116845022
8	82133613	82133614	C		7	GENIC	homozygous	128606822
8	82134556	82134557	C	A	60	GENIC	heterozygous	131060278
8	82134952	82134953	C	A	72	GENIC	heterozygous	131060280
8	82134974	82134975	G	T	70	GENIC	heterozygous	131060281
8	82134984	82134985	T	C	68	GENIC	heterozygous	131060282
8	82134998	82134999	T	A	62	GENIC	heterozygous	131060283
8	82134999	82135000	A	T	62	GENIC	heterozygous	131060284
8	82135084	82135085	A	C	35	GENIC	heterozygous	128662180
8	82135092	82135093	A		30	GENIC	heterozygous	128606823
8	82135120	82135121	C	T	27	GENIC	heterozygous	128662181
8	82135518	82135519	C	G	66	GENIC	heterozygous	117113517
8	82135657	82135658	G	T	37	GENIC	possibly homozygous	116530546