chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	3118274	3118275	G	C	20	GENIC	homozygous	53768143
7	3118599	3118600	C	T	21	GENIC	possibly homozygous	53768145
7	3118800	3118801	T	C	24	GENIC	homozygous	53768147
7	3119277	3119278	G	A	17	GENIC	possibly homozygous	53768153
7	3121427	3121428	G	C	1	GENIC	homozygous	53768159
7	3121544	3121545	G	A	5	GENIC	homozygous	53768161
7	3121690	3121691	A	G	16	GENIC	homozygous	53768163
7	3121740	3121741	T	C	16	GENIC	possibly homozygous	53768165
7	3122529	3122530	G	GA	5	GENIC	homozygous	53768167
7	3123862	3123863	G	GT	1	GENIC	homozygous	53768169
7	3125341	3125342	G	A	6	GENIC	homozygous	53768178
7	3125911	3125912	T	C	2	GENIC	heterozygous	53768183
7	3125921	3125922	T	C	6	GENIC	heterozygous	53768185
7	3128151	3128152	A	ACACAGGGAGATCCCTGGGCT	2	GENIC	homozygous	53768189
7	3128656	3128657	C	G	18	GENIC	heterozygous	53768193
7	3131429	3131430	C	T	18	GENIC	heterozygous	53768199
7	3133229	3133230	T	TC	6	GENIC	heterozygous	53768202
7	3134742	3134743	G	A	28	GENIC	possibly homozygous	53768204
7	3135010	3135011	C	CCGCCG	2	GENIC	homozygous	53768206
7	3138742	3138743	G	A	7	GENIC	homozygous	53768216
7	3139875	3139876	G	A	28	GENIC	possibly homozygous	53768218
7	3140111	3140112	T	C	29	GENIC	homozygous	53768220
7	3141402	3141403	A	ACGGAGGGTGT	7	GENIC	heterozygous	53768222