chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51023062	51023063	C	G	46	GENIC	heterozygous	118450732
13	51023064	51023065	T	G	34	GENIC	homozygous	115100753
13	51023554	51023555	T	C	29	GENIC	homozygous	114342367
13	51023783	51023784	G	T	32	GENIC	homozygous	114342369
13	51024364	51024365	T	C	52	GENIC	homozygous	114342371
13	51024592	51024593	T	C	30	GENIC	homozygous	114342373
13	51025241	51025242	A	T	21	GENIC	homozygous	114342375
13	51026402	51026403	G	A	43	GENIC	homozygous	114342377
13	51027431	51027432	G	A	23	GENIC	homozygous	114342379
13	51028237	51028238	A	T	29	GENIC	homozygous	114672249
13	51029367	51029368	A	T	27	GENIC	homozygous	114342381
13	51029669	51029670	A	G	28	GENIC	homozygous	114342383
13	51029671	51029672	G	A	29	GENIC	homozygous	114342385
13	51029870	51029871	A	G	28	GENIC	homozygous	114342387
13	51030556	51030557	T	C	29	GENIC	homozygous	114342389