chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	109955603	109955604	A	C	89	GENIC	homozygous	138180209
7	109955853	109955853		GTGCTTCTCGGAA	51	GENIC	homozygous	137973835
7	109955961	109955962	T	C	59	GENIC	homozygous	138180210
7	109956421	109956422	T	C	51	GENIC	homozygous	138180211
7	109956658	109956659	A	G	53	GENIC	homozygous	138180212
7	109956725	109956726	C	A	48	GENIC	homozygous	138180213
7	109956771	109956772	C	G	46	GENIC	homozygous	138180214
7	109956879	109956880	T	C	50	GENIC	homozygous	138180215
7	109956912	109956913	G	A	49	GENIC	homozygous	138180216
7	109956961	109956968	GACCTCA		53	GENIC	homozygous	137973836
7	109956990	109956991	A	G	57	GENIC	homozygous	138180217
7	109957076	109957077	A	G	42	GENIC	homozygous	138180218
7	109957102	109957103	G	A	34	GENIC	homozygous	138180219
7	109957130	109957130		TT	23	GENIC	possibly homozygous	137973837
7	109957196	109957197	A	G	29	GENIC	homozygous	138180220
7	109957490	109957491	C	T	50	GENIC	homozygous	138180221
7	109957587	109957588	T	C	49	GENIC	homozygous	138180222
7	109957663	109957663		TTTTGAGACGG	45	GENIC	homozygous	137973839
7	109957717	109957718	C	T	55	GENIC	homozygous	138180223
7	109957900	109957901	A	G	54	GENIC	homozygous	138180224
7	109958133	109958137	CTCT		58	GENIC	homozygous	137973840
7	109958743	109958744	T	C	73	GENIC	homozygous	138180225
7	109961899	109961899		C	58	GENIC	homozygous	137973841
7	109957612	109957613	A		42	GENIC	homozygous	403222113
7	109957612	109957613	A	T	42	GENIC	heterozygous	154488287
7	109959462	109959463	C	G	50	GENIC	homozygous	138180226
7	109960043	109960044	T	C	40	GENIC	homozygous	138180227
7	109960476	109960477	C	T	66	GENIC	homozygous	138180228
7	109961575	109961576	G	A	50	GENIC	possibly homozygous	138180229
7	109961940	109961941	A	G	75	GENIC	homozygous	138180230