chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	121211996	121211997	C	A	25	GENIC	homozygous	137605324
5	121212271	121212272	C	T	28	GENIC	homozygous	137605325
5	121213362	121213363	T	C	21	GENIC	homozygous	137605326
5	121213408	121213409	G	T	23	GENIC	homozygous	137605327
5	121215436	121215437	C		17	GENIC	homozygous	137337464
5	121217351	121217352	G	A	26	GENIC	homozygous	137605328
5	121220511	121220512	G	C	27	GENIC	homozygous	137605329
5	121221227	121221228	A	G	20	GENIC	homozygous	137605330
5	121222495	121222496	G	A	24	GENIC	homozygous	137605331
5	121222812	121222813	T	C	35	GENIC	homozygous	137605332
5	121223018	121223018		AAACA	17	GENIC	homozygous	137337465
5	121227733	121227734	T	A	30	GENIC	homozygous	137605333
5	121228597	121228598	C		8	GENIC	homozygous	137337466
5	121229116	121229117	C	T	11	GENIC	homozygous	137605334
5	121229961	121229961		T	17	GENIC	homozygous	137337472
5	121230286	121230287	G	A	24	GENIC	homozygous	137605335
5	121230318	121230319	G	A	21	GENIC	homozygous	137605336
5	121230645	121230646	T	G	16	GENIC	homozygous	137605337
5	121231243	121231244	G	A	20	GENIC	homozygous	137605338
5	121232115	121232116	A		16	GENIC	homozygous	137337473
5	121232221	121232222	G		23	GENIC	homozygous	137337474
5	121232472	121232472		G	28	GENIC	homozygous	137337475
5	121233478	121233479	G	T	22	GENIC	possibly homozygous	137605339
5	121232115	121232116	A	G	16	GENIC	heterozygous	154330647