chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	101527092	101527093	T	G	47	GENIC	homozygous	118908890
5	101528394	101528397	ATA		40	GENIC	homozygous	132077696
5	101529944	101529945	C	T	25	GENIC	homozygous	118908892
5	101531970	101531971	C	T	44	GENIC	homozygous	118908894
5	101532475	101532476	T		40	GENIC	possibly homozygous	132077697
5	101533949	101533950	A	G	16	GENIC	homozygous	113941724
5	101536413	101536414	A	G	49	GENIC	homozygous	113941728
5	101540897	101540920	TCAGAGTCAATCCAATCAGCCAT		41	GENIC	homozygous	132077698
5	101541910	101541911	T	C	41	GENIC	homozygous	113941734
5	101537950	101537951	C	T	40	GENIC	homozygous	118908896
5	101540556	101540557	C	T	48	GENIC	homozygous	118908898
5	101541536	101541537	T	C	52	GENIC	homozygous	118908900
5	101532626	101532627	G	C	59	GENIC	homozygous	132088248
5	101538630	101538630		T	51	GENIC	possibly homozygous	128218253
5	101543338	101543339	G	A	55	GENIC	homozygous	118908902
5	101544803	101544804	A	G	46	GENIC	homozygous	126259404
5	101545664	101545665	A	T	44	GENIC	homozygous	118908904
5	101546302	101546303	G	A	46	GENIC	homozygous	118908906
5	101548701	101548702	A	G	61	GENIC	homozygous	118908908
5	101549512	101549513	G	T	66	GENIC	possibly homozygous	118908910
5	101552852	101552853	C	T	49	GENIC	homozygous	118908912