chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130218295	130218296	A		34	GENIC	possibly homozygous	137983772
7	130218295	130218296	A	T	34	GENIC	heterozygous	403227151
7	130220884	130220885	G	C	55	GENIC	homozygous	145641320
7	130219044	130219045	G	C	53	GENIC	homozygous	145641317
7	130220199	130220200	T	C	36	GENIC	homozygous	145641318
7	130220881	130220882	A	G	54	GENIC	homozygous	145641319
7	130219875	130219876	C	T	44	GENIC	possibly homozygous	146460020
7	130218845	130218846	G	C	66	GENIC	homozygous	146460019
7	130219876	130219877	C	T	39	GENIC	homozygous	146460021
7	130220347	130220348	C	T	43	GENIC	possibly homozygous	146460022
7	130221121	130221122	G	A	25	GENIC	heterozygous	154490999
7	130221121	130221122	G		25	GENIC	possibly homozygous	403227152
7	130221125	130221126	G	A	25	GENIC	heterozygous	154491000
7	130221593	130221594	G	A	48	GENIC	possibly homozygous	145641321
7	130221594	130221595	C	T	48	GENIC	possibly homozygous	145641322
7	130221127	130221128	G		25	GENIC	possibly homozygous	404005046
7	130221125	130221126	G		25	GENIC	possibly homozygous	404005044
7	130221127	130221128	G	A	25	GENIC	heterozygous	404005045