chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	52159444	52159445	C	-	11	GENIC	possibly homozygous	50249497
12	52159974	52159975	T	C	16	GENIC	possibly homozygous	50249499
12	52160607	52160608	G	A	24	GENIC	homozygous	50249501
12	52160645	52160646	C	T	18	GENIC	homozygous	50249503
12	52160742	52160743	T	C	21	GENIC	homozygous	50249505
12	52161235	52161236	T	C	15	GENIC	heterozygous	50473351
12	52161746	52161747	A	G	21	GENIC	homozygous	50249507
12	52162407	52162408	C	T	6	GENIC	heterozygous	50593875
12	52162471	52162472	A	C	11	GENIC	heterozygous	50249509
12	52164615	52164616	G	GTC	1	GENIC	homozygous	50249517
12	52165474	52165475	A	C	13	GENIC	homozygous	50473352
12	52166427	52166428	T	C	13	GENIC	possibly homozygous	50249553
12	52167559	52167565	TCTGTC	------	4	GENIC	homozygous	50249559
12	52167996	52167997	T	C	7	GENIC	homozygous	50249593
12	52168872	52168873	A	G	15	GENIC	possibly homozygous	50249601
12	52169125	52169126	G	GAC	20	GENIC	homozygous	50249603
12	52169345	52169346	G	T	10	GENIC	possibly homozygous	50473353
12	52169839	52169840	C	T	28	GENIC	possibly homozygous	50249607
12	52169903	52169904	T	C	21	GENIC	possibly homozygous	50473354
12	52170597	52170598	A	G	16	GENIC	possibly homozygous	50249609