chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	147803989	147803991	CC		82	GENIC	homozygous	128253962
5	147805155	147805156	T	C	55	GENIC	homozygous	114047380
5	147805333	147805334	A	C	50	GENIC	homozygous	114047382
5	147805352	147805352		A	45	GENIC	homozygous	128253963
5	147805356	147805357	A		41	GENIC	homozygous	128253964
5	147805500	147805501	G		47	GENIC	homozygous	128253965
5	147805883	147805884	G	A	53	GENIC	homozygous	114047384
5	147806880	147806880		A	51	GENIC	possibly homozygous	128253966
5	147807611	147807612	T	C	55	GENIC	possibly homozygous	114047386
5	147809187	147809188	A	G	37	GENIC	homozygous	114047388
5	147809230	147809231	T	C	23	GENIC	homozygous	122415376
5	147809815	147809816	C	G	30	GENIC	homozygous	114047390
5	147810036	147810037	A	T	49	GENIC	homozygous	114047392
5	147810064	147810067	CTC		47	GENIC	homozygous	128253968
5	147810187	147810188	T	G	54	GENIC	homozygous	114047394
5	147810259	147810260	T	G	62	GENIC	homozygous	114047396
5	147810358	147810359	G	A	54	GENIC	homozygous	114047398
5	147810632	147810633	A		46	GENIC	possibly homozygous	128253969
5	147811709	147811710	T	C	62	GENIC	homozygous	114047408
5	147811735	147811736	T	C	56	GENIC	homozygous	114047410
5	147812098	147812099	C	G	66	GENIC	homozygous	114153118
5	147811930	147811931	C	T	57	GENIC	homozygous	114153116
5	147811962	147811963	G	A	55	GENIC	homozygous	114153117