chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	77986398	77986399	T	A	34	GENIC	homozygous	116044241
7	77987608	77987609	C	G	37	GENIC	homozygous	116197108
7	77987754	77987755	A	G	37	GENIC	homozygous	116197110
7	77987763	77987764	A	G	35	GENIC	homozygous	116197112
7	77988168	77988169	G	A	38	GENIC	homozygous	116044259
7	77988227	77988228	C	T	36	GENIC	homozygous	116044261
7	77988885	77988886	G	A	36	GENIC	homozygous	116197114
7	77989703	77989704	T	C	60	GENIC	homozygous	116044265
7	77990090	77990091	G	A	53	GENIC	homozygous	116044271
7	77990185	77990186	G	A	60	GENIC	homozygous	116044273
7	77994193	77994194	G		42	GENIC	homozygous	131679741
7	77994245	77994246	A	G	52	GENIC	homozygous	116044277
7	77994806	77994807	G	A	49	GENIC	homozygous	116197116
7	77994856	77994857	A	T	41	GENIC	homozygous	116044281
7	77995299	77995300	T	G	49	GENIC	possibly homozygous	116197118
7	77997334	77997335	T	C	37	GENIC	homozygous	116197120
7	77999796	77999797	A	G	45	GENIC	homozygous	116197122
7	78000465	78000466	T	C	36	GENIC	possibly homozygous	116044295
7	78000564	78000565	G	T	37	GENIC	homozygous	116044299
7	78000610	78000611	A	T	32	GENIC	homozygous	116197124
7	78001398	78001399	A	G	43	GENIC	homozygous	116044303
7	77992583	77992584	G	A	2	GENIC	heterozygous	132117665
7	77996942	77996944	TC		40	GENIC	homozygous	132109811
7	77999080	77999084	AAAC		41	GENIC	homozygous	132109812