chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409873414098735GT31GENICheterozygous115262267
121409896214098963TA48GENICpossibly homozygous115262269
121409946514099466GA34GENIChomozygous115262271
121410192014101921AG27GENIChomozygous115262273
121410228514102286CT23GENIChomozygous115262275
121410687914106880AG48GENIChomozygous115262277
121413370114133702GC15GENIChomozygous115262279
121413371214133713GT12GENIChomozygous115262281
121413470214134703TG49GENIChomozygous115262283
121413794614137947GT30GENIChomozygous115262285
121413799614137997TC36GENIChomozygous115262287
121414100414141005GA29GENIChomozygous115262289
121414101714141018AG29GENIChomozygous115262291
121414172314141724AT36GENIChomozygous115262293
121414393814143939AG45GENIChomozygous115262295
121414457614144577AC32GENIChomozygous115262297
121414560614145607CT39GENIChomozygous115262299
121414608314146084AC56GENIChomozygous115262301
121414645914146460TC43GENIChomozygous115262303
121414705214147053TC44GENIChomozygous115262305
121414729114147292TC27GENIChomozygous115262307
121414791614147917CT55GENIChomozygous115262309
121414834914148350GT37GENIChomozygous115262311
121414858714148588GT34GENIChomozygous115262313
121414860614148607TC35GENIChomozygous115262315
121414865914148660CT38GENIChomozygous115262317
121414954614149547TA57GENIChomozygous115262319
121415301814153019GA31GENIChomozygous115262321
121415647814156479CA23GENIChomozygous115262323