chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2517764	2517765	A	T	19	GENIC	heterozygous	115234572
12	2517888	2517889	G	A	24	GENIC	heterozygous	115234574
12	2519768	2519769	A	G	26	GENIC	heterozygous	115234576
12	2519795	2519796	C	T	28	GENIC	heterozygous	115234578
12	2520348	2520349	C	T	16	GENIC	heterozygous	115234580
12	2521580	2521581	C	G	23	GENIC	heterozygous	115234582
12	2521771	2521772	C	T	17	GENIC	heterozygous	115357452
12	2521787	2521788	A	C	15	GENIC	heterozygous	115357453
12	2522278	2522279	T	C	13	GENIC	heterozygous	115357454
12	2526084	2526085	T	C	18	GENIC	heterozygous	115234584
12	2526753	2526754	T	C	23	GENIC	heterozygous	115234586
12	2528072	2528073	A	T	26	GENIC	heterozygous	115234588
12	2528124	2528125	A	T	20	GENIC	heterozygous	115234590
12	2528439	2528440	C	G	15	GENIC	heterozygous	115234592
12	2528448	2528449	A	G	17	GENIC	heterozygous	115234594
12	2531748	2531749	A	G	18	GENIC	heterozygous	115234596
12	2532308	2532309	G	A	13	GENIC	heterozygous	115234598
12	2533065	2533066	C	G	20	GENIC	heterozygous	115234600
12	2533288	2533289	C	T	23	GENIC	heterozygous	115234602
12	2533488	2533489	C	A	17	GENIC	heterozygous	115234604
12	2520793	2520803	TGTATGTATG		21	GENIC	heterozygous	128949569
12	2529733	2529737	ATAT		20	GENIC	heterozygous	128949570
12	2532191	2532192	A	G	17	GENIC	heterozygous	115535444