chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	60436476	60436477	T	C	41	GENIC	possibly homozygous	114365531
13	60437247	60437252	ACAAC		59	GENIC	homozygous	132172122
13	60438306	60438307	C	T	49	GENIC	homozygous	114624755
13	60437733	60437734	C	G	49	GENIC	homozygous	114624749
13	60437932	60437933	A	C	44	GENIC	homozygous	114624751
13	60437934	60437935	C	G	43	GENIC	homozygous	114624753
13	60438495	60438496	C	T	59	GENIC	homozygous	114624757
13	60438529	60438530	A	T	67	GENIC	homozygous	114365532
13	60439184	60439185	G	A	54	GENIC	homozygous	114624759
13	60439414	60439414		A	20	GENIC	possibly homozygous	132172123
13	60439964	60439965	A		44	GENIC	homozygous	132172124
13	60440214	60440215	G	A	73	GENIC	homozygous	114624761
13	60440555	60440556	G	T	65	GENIC	possibly homozygous	114624763
13	60440648	60440649	C	T	60	GENIC	homozygous	114624765
13	60440651	60440652	A	G	61	GENIC	homozygous	114624767
13	60442298	60442299	G	A	45	GENIC	homozygous	114624769
13	60443214	60443215	A	G	63	GENIC	homozygous	114624771
13	60443224	60443225	G	A	57	GENIC	homozygous	114624773
13	60443389	60443390	G	A	44	GENIC	homozygous	114624775
13	60443561	60443562	T	C	63	GENIC	homozygous	114365536
13	60444834	60444835	A	G	54	GENIC	homozygous	114624777
13	60438319	60438323	AGAT		47	GENIC	homozygous	129061258
13	60439357	60439359	TG		24	GENIC	heterozygous	132341467