chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	137253641	137253642	G	A	26	GENIC	homozygous	137632602
5	137253876	137253877	T	A	16	GENIC	homozygous	137632603
5	137254142	137254143	T	G	15	GENIC	homozygous	137632604
5	137255545	137255546	T	C	26	GENIC	homozygous	137632605
5	137259956	137259957	C	T	17	GENIC	homozygous	137632606
5	137261171	137261172	G	T	23	GENIC	possibly homozygous	137632607
5	137268262	137268263	C	T	33	GENIC	homozygous	137632609
5	137268361	137268362	C	T	44	GENIC	homozygous	137632610
5	137268802	137268803	T	G	36	GENIC	homozygous	137632611
5	137269102	137269103	T	C	22	GENIC	homozygous	137632612
5	137269274	137269275	C	T	30	GENIC	homozygous	137632613
5	137271910	137271911	G	A	27	GENIC	homozygous	137632614
5	137272231	137272232	A	G	16	GENIC	homozygous	137632616
5	137272699	137272700	C	T	20	GENIC	homozygous	137632617
5	137272719	137272720	C	A	21	GENIC	homozygous	137632618
5	137273040	137273041	T	A	16	GENIC	homozygous	137632619
5	137273079	137273080	A	G	14	GENIC	homozygous	137632620
5	137273246	137273247	A	T	24	GENIC	homozygous	137632621
5	137273247	137273248	A	T	24	GENIC	homozygous	137632622
5	137272535	137272537	CA		13	GENIC	homozygous	137344494
5	137259381	137259382	T	C	21	GENIC	possibly homozygous	143963586
5	137259385	137259385		TCT	21	GENIC	possibly homozygous	143944808
5	137259381	137259382	T		21	GENIC	heterozygous	403159786