chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409896214098963TA23GENIChomozygous115262269
121410192014101921AG31GENIChomozygous115262273
121410228514102286CT23GENIChomozygous115262275
121410687914106880AG33GENIChomozygous115262277
121413470214134703TG26GENIChomozygous115262283
121413794614137947GT28GENIChomozygous115262285
121413799614137997TC27GENIChomozygous115262287
121414100414141005GA32GENIChomozygous115262289
121414101714141018AG30GENIChomozygous115262291
121414172314141724AT39GENIChomozygous115262293
121414393814143939AG26GENIChomozygous115262295
121414457614144577AC25GENIChomozygous115262297
121414560614145607CT21GENIChomozygous115262299
121414608314146084AC21GENIChomozygous115262301
121414645914146460TC26GENIChomozygous115262303
121414705214147053TC23GENIChomozygous115262305
121414729114147292TC26GENIChomozygous115262307
121414743514147436CT36GENIChomozygous115417741
121414791614147917CT32GENIChomozygous115262309
121414834914148350GT30GENIChomozygous115262311
121414858714148588GT28GENIChomozygous115262313
121414860614148607TC29GENIChomozygous115262315
121414865914148660CT35GENIChomozygous115262317
121414954614149547TA29GENIChomozygous115262319
121414467614144677CT35GENIChomozygous115437979
121414659814146599AG25GENIChomozygous115437980
121415301814153019GA21GENIChomozygous115262321