chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	131090612	131090613	T	C	28	GENIC	homozygous	52896194
8	131091216	131091217	T	C	17	GENIC	homozygous	53065537
8	131093978	131093979	G	C	26	GENIC	homozygous	52896204
8	131094058	131094059	A	G	35	GENIC	homozygous	52896207
8	131097872	131097873	C	CACATGTCACACAGATCTGTCTGAGCTCAGCTCACACATGTCACACAGATCCATCTGTGCTCAGCTCAT	71	GENIC	possibly homozygous	53415948
8	131101188	131101189	A	C	49	GENIC	homozygous	53065553
8	131101237	131101238	A	C	34	GENIC	homozygous	53065554
8	131103227	131103228	T	C	30	GENIC	homozygous	53065555
8	131103302	131103303	T	C	27	GENIC	homozygous	53065556
8	131103494	131103495	C	G	17	GENIC	homozygous	53065557
8	131104227	131104228	C	A	20	GENIC	homozygous	53065558
8	131104625	131104626	T	G	26	GENIC	homozygous	53065559
8	131104828	131104830	GT	--	5	GENIC	homozygous	53415949
8	131105633	131105634	T	C	28	GENIC	homozygous	52896315