chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	140563631	140563632	G	C	35	GENIC	homozygous	114030600
5	140564326	140564327	A	G	23	GENIC	homozygous	114030601
5	140565915	140565916	T	C	37	GENIC	homozygous	114148919
5	140566047	140566048	T	G	24	GENIC	homozygous	114030603
5	140567581	140567582	G	A	12	GENIC	homozygous	114030604
5	140569024	140569025	T	C	34	GENIC	homozygous	114030605
5	140569049	140569050	G	A	28	GENIC	homozygous	114030606
5	140569060	140569061	T	C	24	GENIC	homozygous	114030607
5	140569276	140569277	T	C	36	GENIC	homozygous	114030608
5	140569470	140569471	G	A	24	GENIC	homozygous	114030609
5	140570672	140570673	A	G	27	GENIC	homozygous	114030610
5	140572393	140572394	T	C	17	GENIC	homozygous	114030611
5	140572986	140572987	G	A	18	GENIC	homozygous	114030612
5	140573561	140573562	G	C	30	GENIC	homozygous	114030617
5	140574848	140574849	T	C	28	GENIC	homozygous	114030618
5	140575929	140575930	G	A	10	GENIC	homozygous	114030619
5	140576503	140576504	G	T	34	GENIC	homozygous	114030620
5	140583111	140583112	A	G	33	GENIC	homozygous	114030622
5	140584349	140584350	G	C	37	GENIC	homozygous	114030623