chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4161685619161685620TG7GENIChomozygous119320100
4161685935161685936CA5GENIChomozygous119320101
4161686829161686830GA10GENIChomozygous112919644
4161686876161686877AG11GENIChomozygous119320102
4161686957161686958AG8GENIChomozygous119320103
4161687777161687778TC5GENIChomozygous119320104
4161688055161688056AC15GENIChomozygous119320105
4161688617161688618AG6GENIChomozygous119320106
4161689229161689230AT7GENIChomozygous119320107
4161689990161689991TG10GENIChomozygous119320108
4161690011161690012TC12GENIChomozygous119320109
4161691136161691137CT15GENIChomozygous119320110
4161691341161691342TG16GENIChomozygous119320111
4161691454161691455AG12GENIChomozygous119320112
4161692083161692084CG9GENIChomozygous119320113
4161692171161692172AG7GENIChomozygous119320114
4161696068161696069GA11GENIChomozygous119320115
4161696233161696234TC10GENIChomozygous119320116
4161697404161697405TC9GENIChomozygous119320117