chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	136733687	136733688	T	C	30	GENIC	homozygous	114020631
5	136734219	136734220	T	C	34	GENIC	possibly homozygous	114020633
5	136734846	136734847	G	A	16	GENIC	homozygous	114020635
5	136735308	136735309	C	A	21	GENIC	homozygous	114020637
5	136735435	136735436	G	A	17	GENIC	homozygous	114020639
5	136737742	136737743	G	A	20	GENIC	homozygous	114535937
5	136738047	136738048	A	G	24	GENIC	homozygous	114020642
5	136739230	136739231	A	C	31	GENIC	homozygous	114020644
5	136739411	136739412	C	T	21	GENIC	homozygous	114020646
5	136740341	136740342	T	C	23	GENIC	homozygous	114020648
5	136740572	136740573	A	G	30	GENIC	homozygous	114020650
5	136740810	136740811	C	T	26	GENIC	homozygous	114020652
5	136740912	136740913	G	A	28	GENIC	homozygous	114020654
5	136744018	136744019	A	G	32	GENIC	homozygous	114535943
5	136744959	136744960	G	A	26	GENIC	homozygous	114020662
5	136745297	136745298	G	A	23	GENIC	homozygous	114535945
5	136746896	136746897	G	A	34	GENIC	homozygous	114020664
5	136747767	136747768	A	G	19	GENIC	homozygous	114020668
5	136748497	136748498	C	A	8	GENIC	homozygous	114020670