chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	60436476	60436477	T	C	13	GENIC	homozygous	114365531
13	60437247	60437252	ACAAC		16	GENIC	homozygous	132172122
13	60437733	60437734	C	G	26	GENIC	homozygous	114624749
13	60437932	60437933	A	C	13	GENIC	homozygous	114624751
13	60437934	60437935	C	G	13	GENIC	homozygous	114624753
13	60438306	60438307	C	T	22	GENIC	homozygous	114624755
13	60438319	60438323	AGAT		21	GENIC	homozygous	129061258
13	60438495	60438496	C	T	15	GENIC	possibly homozygous	114624757
13	60438529	60438530	A	T	14	GENIC	homozygous	114365532
13	60439184	60439185	G	A	22	GENIC	homozygous	114624759
13	60439357	60439359	TG		6	GENIC	heterozygous	132341467
13	60439964	60439965	A		14	GENIC	homozygous	132172124
13	60440214	60440215	G	A	32	GENIC	homozygous	114624761
13	60440555	60440556	G	T	21	GENIC	homozygous	114624763
13	60440648	60440649	C	T	23	GENIC	homozygous	114624765
13	60440651	60440652	A	G	24	GENIC	homozygous	114624767
13	60442298	60442299	G	A	26	GENIC	homozygous	114624769
13	60443214	60443215	A	G	26	GENIC	homozygous	114624771
13	60443224	60443225	G	A	29	GENIC	homozygous	114624773
13	60443389	60443390	G	A	18	GENIC	homozygous	114624775
13	60443561	60443562	T	C	17	GENIC	homozygous	114365536
13	60444834	60444835	A	G	21	GENIC	homozygous	114624777