chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2517764	2517765	A	T	23	GENIC	homozygous	115234572
12	2517888	2517889	G	A	31	GENIC	homozygous	115234574
12	2520348	2520349	C	T	21	GENIC	homozygous	115234580
12	2521580	2521581	C	G	23	GENIC	homozygous	115234582
12	2521771	2521772	C	T	18	GENIC	homozygous	115357452
12	2521787	2521788	A	C	21	GENIC	homozygous	115357453
12	2526084	2526085	T	C	21	GENIC	homozygous	115234584
12	2526753	2526754	T	C	18	GENIC	homozygous	115234586
12	2528072	2528073	A	T	31	GENIC	homozygous	115234588
12	2528124	2528125	A	T	28	GENIC	homozygous	115234590
12	2528439	2528440	C	G	19	GENIC	homozygous	115234592
12	2528448	2528449	A	G	20	GENIC	homozygous	115234594
12	2531748	2531749	A	G	25	GENIC	homozygous	115234596
12	2532308	2532309	G	A	12	GENIC	homozygous	115234598
12	2533065	2533066	C	G	15	GENIC	homozygous	115234600
12	2533288	2533289	C	T	21	GENIC	homozygous	115234602
12	2533488	2533489	C	A	17	GENIC	homozygous	115234604