chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25012649	25012650	T	C	36	GENIC	homozygous	115368998
12	25012725	25012726	T	A	39	GENIC	homozygous	115369000
12	25013007	25013008	A	G	20	GENIC	homozygous	115581751
12	25013674	25013675	G	A	26	GENIC	homozygous	115438914
12	25013826	25013827	G	A	24	GENIC	homozygous	115369002
12	25013926	25013927	A	G	30	GENIC	homozygous	118325039
12	25014166	25014167	C	T	35	GENIC	homozygous	115369004
12	25014467	25014468	C	T	36	GENIC	homozygous	115369006
12	25014720	25014721	T	C	36	GENIC	homozygous	115369008
12	25015260	25015261	G	A	45	GENIC	homozygous	115369010
12	25015302	25015305	AAC		44	GENIC	homozygous	131115616
12	25013009	25013009		T	20	GENIC	homozygous	131115611
12	25013271	25013271		AC	22	GENIC	homozygous	131115612
12	25013790	25013794	TACC		22	GENIC	homozygous	131115613
12	25014922	25014924	CA		25	GENIC	homozygous	131115614
12	25014939	25014941	AT		21	GENIC	homozygous	131115615
12	25013297	25013298	G	A	23	GENIC	homozygous	115470203
12	25015001	25015002	C	T	30	GENIC	homozygous	115470205
12	25013441	25013442	C	T	3	GENIC	heterozygous	132708199
12	25013444	25013445	T	A	3	GENIC	heterozygous	132708200
12	25013475	25013476	G	A	10	GENIC	homozygous	115422786
12	25015421	25015421		GGGGCTGGTGGCGTGGCT	18	GENIC	homozygous	131115617
12	25015449	25015450	G		25	GENIC	homozygous	131115618
12	25015597	25015598	T	C	38	GENIC	homozygous	115369012
12	25015619	25015620	A	G	41	GENIC	homozygous	115369014
12	25015730	25015731	G	A	42	GENIC	homozygous	115369016
12	25016225	25016226	G	A	35	GENIC	homozygous	115369018
12	25016332	25016350	GGAGGACTTGGTGGGCCC		26	GENIC	homozygous	131115619
12	25016374	25016375	C	T	30	GENIC	homozygous	115369020
12	25016391	25016392	A	T	31	GENIC	homozygous	115369022
12	25017254	25017255	T	C	44	GENIC	homozygous	115289388
12	25021709	25021710	G	T	39	GENIC	possibly homozygous	115369024