chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14033580	14033583	TTT	---	8	GENIC	possibly homozygous	51622642
10	14033603	14033604	C	CT	13	GENIC	heterozygous	51622643
10	14034061	14034062	T	C	20	GENIC	homozygous	51622644
10	14034207	14034208	A	AAT	18	GENIC	homozygous	51622645
10	14034338	14034339	A	-	9	GENIC	homozygous	51622646
10	14034627	14034628	G	A	19	GENIC	homozygous	51622647
10	14034869	14034870	C	A	27	GENIC	homozygous	51622648
10	14035316	14035318	AA	--	5	GENIC	homozygous	51622649
10	14036759	14036760	A	-	12	GENIC	homozygous	51622650
10	14037333	14037334	G	C	23	GENIC	homozygous	51622651
10	14039205	14039206	T	C	20	GENIC	homozygous	51622652
10	14041046	14041052	GTGTGT	------	4	GENIC	homozygous	51622653
10	14043753	14043754	A	G	24	GENIC	homozygous	51622655
10	14044236	14044237	T	C	15	GENIC	homozygous	51622656
10	14044937	14044941	TTTG	----	20	GENIC	homozygous	51622657
10	14045329	14045330	G	A	28	GENIC	homozygous	51622658
10	14045400	14045401	T	TTCCTGGGAGC	17	GENIC	homozygous	51622659