chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1243354543243354544CA49GENIChomozygous135852702
1243354766243354767GA55GENIChomozygous135852703
1243354777243354778CT56GENIChomozygous135852704
1243355813243355814CT50GENIChomozygous135852705
1243355968243355969GA51GENIChomozygous145339216
1243358061243358062TC35GENIChomozygous135852706
1243358286243358286CCT11GENIChomozygous135469783
1243358364243358365TC15GENIChomozygous135852707
1243359350243359351AG44GENIChomozygous135852708
1243360343243360344GA45GENIChomozygous135852709
1243360762243360763TC37GENIChomozygous135852710
1243361243243361244GA43GENIChomozygous135852711
1243362637243362638AG40GENIChomozygous135852712
1243365263243365281CACACACATACACACACT15GENICheterozygous135469784
1243365264243365265A15GENICheterozygous404410416
1243365264243365265AG15GENICheterozygous404410417
1243369686243369687TG39GENIChomozygous145339217
1243371587243371588CT38GENIChomozygous141305565
1243371709243371710TC42GENICpossibly homozygous145339218
1243375258243375259CT51GENIChomozygous145339222
1243372706243372707CT58GENIChomozygous145339219
1243374100243374101TC51GENIChomozygous145339220
1243374781243374782AT35GENIChomozygous145339221
1243368723243368733TGTGTGTTTG6GENIChomozygous147730551
1243368777243368789TGTGTGTGTTTG7GENICpossibly homozygous147730552