chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120418344	120418345	T	G	62	GENIC	homozygous	138197242
7	120418474	120418475	G	A	56	GENIC	homozygous	138197243
7	120419146	120419147	C	A	75	GENIC	homozygous	138197244
7	120419223	120419224	C	T	72	GENIC	homozygous	138197245
7	120419296	120419297	C	T	68	GENIC	homozygous	138197246
7	120419491	120419492	A	C	43	GENIC	homozygous	138197247
7	120419987	120419988	C	T	56	GENIC	homozygous	138197248
7	120420526	120420527	T	G	61	GENIC	homozygous	138197249
7	120420588	120420589	T	C	55	GENIC	homozygous	138197250
7	120420652	120420653	T	A	46	GENIC	homozygous	138197251
7	120421000	120421001	G	C	10	GENIC	homozygous	138197252
7	120421005	120421006	T	C	8	GENIC	homozygous	138197253
7	120421091	120421092	G	A	28	GENIC	homozygous	138197254
7	120421115	120421116	C	T	37	GENIC	homozygous	138197255
7	120421271	120421272	C	T	48	GENIC	homozygous	138197256
7	120421329	120421330	C	A	44	GENIC	possibly homozygous	138197257
7	120421733	120421734	G	A	56	GENIC	homozygous	138197258
7	120421751	120421752	T	C	60	GENIC	homozygous	138197259
7	120422122	120422123	C	T	41	GENIC	homozygous	138197260
7	120422422	120422423	C	T	50	GENIC	homozygous	138197261
7	120422661	120422662	C	T	29	GENIC	homozygous	138197262
7	120422784	120422785	C	T	58	GENIC	homozygous	138197263