chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	14892506	14892507	T	G	66	GENIC	homozygous	115575939
7	14892986	14892987	A	C	32	GENIC	homozygous	115575940
7	14893166	14893167	G	A	36	GENIC	possibly homozygous	115575941
7	14894059	14894060	A	T	49	GENIC	homozygous	115575942
7	14894422	14894423	T	G	42	GENIC	heterozygous	116383632
7	14895986	14895987	C	T	132	GENIC	heterozygous	115575943
7	14896023	14896024	C	T	147	GENIC	heterozygous	115575944
7	14896037	14896038	T	C	138	GENIC	heterozygous	115575945
7	14898528	14898529	T	C	53	GENIC	homozygous	115575946
7	14898536	14898537	T	C	53	GENIC	homozygous	115575947
7	14899297	14899298	A	C	55	GENIC	homozygous	115575948
7	14902265	14902266	G	A	57	GENIC	homozygous	115575949
7	14903983	14903984	T	C	48	GENIC	homozygous	115575950
7	14904873	14904874	G	A	52	GENIC	homozygous	115575951
7	14906518	14906519	G	A	55	GENIC	homozygous	115575952
7	14906573	14906574	G	A	47	GENIC	homozygous	115575953
7	14906640	14906641	A	T	47	GENIC	homozygous	115575954
7	14906708	14906709	C	T	48	GENIC	homozygous	115575955
7	14906711	14906712	T	C	49	GENIC	homozygous	115575956
7	14906810	14906811	C	T	35	GENIC	homozygous	115575957
7	14906825	14906826	A	G	24	GENIC	possibly homozygous	115575958
7	14906834	14906835	C	G	23	GENIC	homozygous	115575959