chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148266721082667211TC18GENIChomozygous113603982
148266745282667453GA34GENIChomozygous113603983
148266996982669970GA14GENIChomozygous113603984
148267012382670124GA27GENIChomozygous113603985
148267012482670125AG26GENIChomozygous113603986
148267086882670869CG18GENIChomozygous113679802
148267122482671225CT22GENIChomozygous113603987
148267133982671340GA29GENIChomozygous113603988
148267143082671431GA32GENIChomozygous113603989
148267344782673448GA18GENIChomozygous113603990
148267351782673518CT21GENIChomozygous113603991
148267458982674590TC26GENIChomozygous113603992
148267533582675336TC25GENIChomozygous113603993
148267584182675842AG16GENIChomozygous113603994
148267609882676099GA22GENICpossibly homozygous113603995
148267759782677598TC17GENIChomozygous113603996
148267887882678879GA16GENIChomozygous113603997
148267939182679392CT31GENIChomozygous113603998
148268076782680768AG24GENIChomozygous113604000
148268084582680846TC26GENIChomozygous113604001
148268271082682711CT33GENIChomozygous113604002
148268303082683031AC36GENIChomozygous113604003
148268315482683155AG24GENIChomozygous113604004
148268411682684117GA16GENIChomozygous113604005
148268487382684874GC34GENIChomozygous113604006
148268635582686356AG32GENIChomozygous113604007
148268706182687062AG27GENIChomozygous113604008
148268841982688420CT21GENIChomozygous113604009
148268921182689212TC21GENIChomozygous113604010
148269130282691303TG17GENIChomozygous113604011
148269132882691329TC20GENIChomozygous113604012
148269149782691498CT19GENIChomozygous113604013
148269246182692462TC35GENIChomozygous113604014
148269356582693566CT29GENIChomozygous113604015
148269379182693792GC24GENIChomozygous113604016
148269428582694286GA23GENIChomozygous113604018
148269507282695073CT18GENIChomozygous113604019
148269606582696066TC23GENIChomozygous113679804