chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25012649	25012650	T	C	25	GENIC	homozygous	115368998
12	25012725	25012726	T	A	21	GENIC	homozygous	115369000
12	25013007	25013008	A	G	10	GENIC	homozygous	115581751
12	25013297	25013298	G	A	10	GENIC	homozygous	115470203
12	25013475	25013476	G	A	12	GENIC	homozygous	115422786
12	25013674	25013675	G	A	15	GENIC	homozygous	115438914
12	25014166	25014167	C	T	27	GENIC	homozygous	115369004
12	25014467	25014468	C	T	24	GENIC	homozygous	115369006
12	25014720	25014721	T	C	28	GENIC	homozygous	115369008
12	25015260	25015261	G	A	30	GENIC	homozygous	115369010
12	25015406	25015407	G	A	4	GENIC	homozygous	115581753
12	25015597	25015598	T	C	14	GENIC	homozygous	115369012
12	25015619	25015620	A	G	16	GENIC	homozygous	115369014
12	25015730	25015731	G	A	17	GENIC	homozygous	115369016
12	25016225	25016226	G	A	25	GENIC	homozygous	115369018
12	25016374	25016375	C	T	25	GENIC	homozygous	115369020
12	25016391	25016392	A	T	28	GENIC	homozygous	115369022
12	25017254	25017255	T	C	22	GENIC	homozygous	115289388
12	25021709	25021710	G	T	25	GENIC	homozygous	115369024