chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1235170566235170567A14GENICheterozygous130217587
1235170570235170571AC15GENICheterozygous109203298
1235170571235170572AC15GENICheterozygous130241195
1235176616235176617A21GENIChomozygous127492649
1235176628235176629CA18GENIChomozygous109203304
1235176629235176630AC18GENIChomozygous109203306
1235176643235176644T17GENIChomozygous127492650
1235176649235176650A17GENIChomozygous127492651
1235176656235176657C15GENIChomozygous127492652
1235176664235176665T14GENIChomozygous127492653
1235176691235176691T10GENIChomozygous127492654
1235176696235176697GT11GENIChomozygous121195649
1235176699235176700T12GENIChomozygous127492655
1235176703235176703G12GENIChomozygous127492656
1235176711235176712G10GENIChomozygous127492657
1235176715235176715C10GENIChomozygous127492658
1235176717235176717A10GENIChomozygous127492659
1235195731235195732TA8GENICheterozygous108568886
1235195782235195783TC9GENICheterozygous108568888
1235196184235196185AT3GENICheterozygous127582330
1235197447235197448AT8GENIChomozygous108568892
1235209941235209942TC20GENIChomozygous125381418
1235321077235321078AT16GENIChomozygous108569203