chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24677809	24677810	C	G	13	GENIC	possibly homozygous	50418513
12	24678256	24678257	G	A	16	GENIC	homozygous	50418514
12	24678381	24678382	C	CA	4	GENIC	heterozygous	50418515
12	24678545	24678546	C	CCTAA	2	GENIC	homozygous	50418516
12	24678703	24678704	T	TAGGCTTGTAC	1	GENIC	homozygous	50293590
12	24679032	24679033	A	G	24	GENIC	homozygous	50293592
12	24679779	24679780	A	G	3	GENIC	heterozygous	50293598
12	24680201	24680202	A	G	28	GENIC	homozygous	50293602
12	24680236	24680237	C	T	15	GENIC	possibly homozygous	50418517
12	24681141	24681142	A	G	17	GENIC	homozygous	50293608
12	24682013	24682014	C	T	7	GENIC	homozygous	50293625
12	24682110	24682114	CTTT	----	1	GENIC	homozygous	50418518
12	24682215	24682216	C	T	10	GENIC	homozygous	50418519
12	24682603	24682604	G	T	11	GENIC	homozygous	50418520
12	24682867	24682868	A	G	20	GENIC	possibly homozygous	50293632
12	24682919	24682920	C	T	8	GENIC	possibly homozygous	50293634
12	24682955	24682956	G	A	13	GENIC	heterozygous	50418521
12	24683147	24683148	C	T	13	GENIC	possibly homozygous	50418522
12	24683397	24683398	C	-	8	GENIC	homozygous	50418523
12	24683399	24683400	C	T	8	GENIC	homozygous	50508226
12	24683831	24683832	A	T	2	GENIC	homozygous	50135700
12	24683834	24683835	G	T	1	GENIC	homozygous	50135702
12	24688106	24688107	T	C	9	GENIC	homozygous	50293686
12	24688226	24688227	T	A	13	GENIC	possibly homozygous	50293688