chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	129798708	129798709	C	T	32	GENIC	homozygous	115888239
7	129799658	129799659	G	A	22	GENIC	homozygous	115888243
7	129800613	129800614	C	T	18	GENIC	homozygous	115888245
7	129801117	129801118	A	G	9	GENIC	homozygous	115888247
7	129801936	129801937	G	A	8	GENIC	homozygous	115888249
7	129804694	129804695	T	G	23	GENIC	homozygous	115888253
7	129804776	129804777	T	C	20	GENIC	homozygous	115888255
7	129804821	129804822	G	A	24	GENIC	homozygous	115888257
7	129805161	129805162	T	C	46	GENIC	homozygous	115888259
7	129805282	129805283	A	G	32	GENIC	homozygous	115888261
7	129805315	129805316	T	C	28	GENIC	homozygous	115888263
7	129805327	129805328	G	T	24	GENIC	homozygous	115888265
7	129806000	129806001	C	T	35	GENIC	homozygous	115888275
7	129806589	129806590	C	T	41	GENIC	homozygous	115888277
7	129807333	129807334	G	A	22	GENIC	homozygous	115888279
7	129807636	129807637	C	A	8	GENIC	homozygous	115888281
7	129808777	129808778	C	T	26	GENIC	homozygous	115888285
7	129808911	129808912	G	T	27	GENIC	homozygous	115888287
7	129808987	129808988	A	G	38	GENIC	homozygous	115888289
7	129810320	129810321	T	C	27	GENIC	homozygous	115888291
7	129810349	129810350	T	C	32	GENIC	homozygous	115888293
7	129810795	129810796	C	T	25	GENIC	homozygous	115888295
7	129810829	129810830	G	A	28	GENIC	homozygous	115888297
7	129811223	129811224	A	G	38	GENIC	homozygous	115888299