chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	94270942	94270943	A	T	9	GENIC	homozygous	49967162
13	94271386	94271387	T	TTTG	8	GENIC	homozygous	49967163
13	94271426	94271427	A	T	10	GENIC	possibly homozygous	49967164
13	94271506	94271507	A	-	18	GENIC	homozygous	49967165
13	94271623	94271624	T	C	13	GENIC	homozygous	49967166
13	94271709	94271710	T	C	6	GENIC	homozygous	49967167
13	94271737	94271738	C	T	7	GENIC	homozygous	49967168
13	94271789	94271790	C	CTTGTCTTTTCTA	7	GENIC	possibly homozygous	49967170
13	94272463	94272464	T	C	26	GENIC	homozygous	49967171
13	94272617	94272620	CTC	---	2	GENIC	homozygous	49967172
13	94272635	94272636	G	-	4	GENIC	heterozygous	49967173
13	94273308	94273309	A	AT	7	GENIC	possibly homozygous	49967174
13	94273329	94273330	G	A	13	GENIC	possibly homozygous	49967175
13	94273811	94273812	G	GA	4	GENIC	homozygous	49967176
13	94273812	94273813	G	T	4	GENIC	homozygous	50497527
13	94273838	94273839	C	T	10	GENIC	homozygous	49967177
13	94274004	94274005	T	C	21	GENIC	homozygous	49967178
13	94274029	94274030	C	T	17	GENIC	possibly homozygous	49967179
13	94274491	94274492	G	A	18	GENIC	possibly homozygous	49967180
13	94274602	94274603	T	C	18	GENIC	possibly homozygous	49967181
13	94274727	94274728	C	A	19	GENIC	homozygous	49967182
13	94274798	94274799	G	A	14	GENIC	homozygous	49967183
13	94274836	94274837	G	A	6	GENIC	heterozygous	49967184
13	94274922	94274923	G	T	12	GENIC	homozygous	49967185
13	94275236	94275237	G	A	16	GENIC	possibly homozygous	49967186
13	94275595	94275596	G	A	11	GENIC	homozygous	49967187
13	94275703	94275704	C	T	21	GENIC	possibly homozygous	49967188
13	94276505	94276506	C	T	20	GENIC	homozygous	49967189