chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	110485585	110485586	T	C	49	GENIC	homozygous	138181278
7	110485616	110485617	G	A	55	GENIC	homozygous	138181279
7	110485690	110485691	A	G	49	GENIC	homozygous	138181280
7	110486611	110486612	G		66	GENIC	homozygous	137974063
7	110486624	110486625	G	A	65	GENIC	homozygous	138181282
7	110486649	110486650	A	G	70	GENIC	homozygous	138181283
7	110486668	110486669	C		56	GENIC	homozygous	137974064
7	110486955	110486961	TTTTTT		7	GENIC	homozygous	137974065
7	110486972	110486973	A	C	16	GENIC	homozygous	138181284
7	110487056	110487062	TTTCTC		45	GENIC	homozygous	137974066
7	110487097	110487098	C	T	56	GENIC	homozygous	138181285
7	110487116	110487117	T	C	59	GENIC	homozygous	138181286
7	110487287	110487288	G	A	54	GENIC	homozygous	138181287
7	110487605	110487606	G	A	70	GENIC	homozygous	138181288
7	110487835	110487836	T	C	71	GENIC	possibly homozygous	138181289
7	110487871	110487872	T	C	68	GENIC	homozygous	138181290
7	110487940	110487941	G	A	72	GENIC	homozygous	138181291
7	110487978	110487979	C	G	68	GENIC	homozygous	138181292
7	110488001	110488002	C	T	73	GENIC	homozygous	138181293
7	110488043	110488044	T	A	72	GENIC	homozygous	138181294
7	110486738	110486739	T	G	59	GENIC	homozygous	143365169
7	110486803	110486804	C	G	52	GENIC	homozygous	143365170