chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3153970	3153971	G	C	34	GENIC	heterozygous	109416933
20	3154393	3154394	G	A	31	GENIC	heterozygous	109370594
20	3154908	3154909	A	G	28	GENIC	possibly homozygous	109416935
20	3155111	3155112	T	C	24	GENIC	heterozygous	109370596
20	3155235	3155236	A	G	35	GENIC	heterozygous	109370598
20	3155624	3155625	A	C	41	GENIC	heterozygous	109505919
20	3155763	3155764	A	G	25	GENIC	heterozygous	109505921
20	3155861	3155862	A	C	29	GENIC	heterozygous	109454568
20	3155911	3155912	G	A	31	GENIC	heterozygous	109454570
20	3155970	3155971	A	G	24	GENIC	heterozygous	109454573
20	3155981	3155982	T	C	23	GENIC	heterozygous	109454575
20	3157144	3157145	G	A	36	GENIC	heterozygous	109605390
20	3157203	3157204	T	A	35	GENIC	heterozygous	109454577
20	3157241	3157242	C	A	26	GENIC	heterozygous	109490451
20	3157315	3157316	G	A	26	GENIC	heterozygous	109490453
20	3157326	3157327	G	A	32	GENIC	heterozygous	109454580
20	3157694	3157695	A	G	32	GENIC	possibly homozygous	109454587
20	3157740	3157741	C	T	31	GENIC	possibly homozygous	109454590
20	3157824	3157825	C	G	33	GENIC	heterozygous	109454592
20	3157888	3157889	C	G	33	GENIC	heterozygous	109605392
20	3158886	3158887	G	T	29	GENIC	heterozygous	109454597
20	3160696	3160697	C	T	24	GENIC	possibly homozygous	109454602
20	3160700	3160701	C	T	25	GENIC	possibly homozygous	109454604
20	3160950	3160951	T	C	28	GENIC	heterozygous	109605395
20	3160953	3160954	T	C	27	GENIC	heterozygous	109605397