chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106377610663776107GC30GENIChomozygous116978560
106377622363776224AG20GENIChomozygous116616464
106377740763777408AG20GENIChomozygous117296018
106377820363778204CA20GENIChomozygous116616468
106377983363779834GT11GENIChomozygous116616470
106377986863779869AC12GENIChomozygous117998296
106378004863780049GT20GENIChomozygous117219632
106378039763780398AC17GENIChomozygous117998297
106378056363780564GT13GENIChomozygous117013227
106378074563780746AT12GENIChomozygous117998298
106378078263780783CT9GENIChomozygous117998299
106378104263781043CG16GENIChomozygous117998302
106378119563781196CG8GENIChomozygous116978562
106378120663781207GT21GENIChomozygous117998303
106378136063781361AC10GENIChomozygous117998304
106378148363781484GT19GENIChomozygous117998305
106378207463782075TC21GENIChomozygous116940697
106378294663782947CT33GENIChomozygous116940699
106378473463784735AT54GENIChomozygous116940701
106378485563784856GA50GENIChomozygous116940703
106378634463786345CT30GENIChomozygous117296022
106378802363788024CT17GENICpossibly homozygous117998306
106378870963788710GC38GENICheterozygous116616486
106378928963789290TC24GENIChomozygous116940705
106378943963789440GT31GENIChomozygous116940707
106379062063790621AC36GENIChomozygous116616490
106379067163790672TC38GENIChomozygous116616492
106379087663790877AG17GENIChomozygous116791575
106379279163792792GA55GENIChomozygous117296024
106379419263794193CT15GENIChomozygous117079966
106379419663794197CT13GENIChomozygous117079967
106379421263794213TC10GENICheterozygous118123932
106379449263794493AC18GENIChomozygous116791577
106379451963794520GC14GENIChomozygous117255898
106379453263794533GC19GENIChomozygous117255900
106379466163794662GT34GENIChomozygous116616496
106379474163794742GC30GENIChomozygous116616498
106379501463795015TC26GENIChomozygous116616502