chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	110485585	110485586	T	C	24	GENIC	homozygous	138181278
7	110485616	110485617	G	A	17	GENIC	homozygous	138181279
7	110485690	110485691	A	G	7	GENIC	homozygous	138181280
7	110486611	110486612	G		13	GENIC	homozygous	137974063
7	110486624	110486625	G	A	13	GENIC	homozygous	138181282
7	110486649	110486650	A	G	11	GENIC	homozygous	138181283
7	110486668	110486669	C		11	GENIC	homozygous	137974064
7	110486738	110486739	T	G	11	GENIC	homozygous	143365169
7	110486803	110486804	C	G	6	GENIC	homozygous	143365170
7	110486972	110486973	A	C	1	GENIC	homozygous	138181284
7	110487056	110487062	TTTCTC		6	GENIC	homozygous	137974066
7	110487097	110487098	C	T	10	GENIC	homozygous	138181285
7	110487116	110487117	T	C	12	GENIC	homozygous	138181286
7	110487287	110487288	G	A	19	GENIC	homozygous	138181287
7	110487605	110487606	G	A	14	GENIC	homozygous	138181288
7	110487835	110487836	T	C	18	GENIC	homozygous	138181289
7	110487871	110487872	T	C	20	GENIC	homozygous	138181290
7	110487940	110487941	G	A	21	GENIC	homozygous	138181291
7	110487978	110487979	C	G	15	GENIC	homozygous	138181292
7	110488001	110488002	C	T	16	GENIC	homozygous	138181293
7	110488043	110488044	T	A	16	GENIC	homozygous	138181294