chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409896214098963TA29GENIChomozygous115262269
121409946514099466GA18GENIChomozygous115262271
121410192014101921AG26GENIChomozygous115262273
121410228514102286CT24GENIChomozygous115262275
121410687914106880AG27GENIChomozygous115262277
121413470214134703TG41GENIChomozygous115262283
121413794614137947GT14GENIChomozygous115262285
121413799614137997TC14GENIChomozygous115262287
121414100414141005GA22GENIChomozygous115262289
121414101714141018AG22GENIChomozygous115262291
121414172314141724AT24GENIChomozygous115262293
121414393814143939AG30GENIChomozygous115262295
121414457614144577AC18GENIChomozygous115262297
121414560614145607CT25GENIChomozygous115262299
121414608314146084AC18GENIChomozygous115262301
121414645914146460TC22GENIChomozygous115262303
121414705214147053TC15GENIChomozygous115262305
121414729114147292TC25GENIChomozygous115262307
121414743514147436CT34GENIChomozygous115417741
121414791614147917CT22GENIChomozygous115262309
121414834914148350GT21GENIChomozygous115262311
121414858714148588GT17GENIChomozygous115262313
121414860614148607TC18GENIChomozygous115262315
121414865914148660CT18GENIChomozygous115262317
121414954614149547TA22GENIChomozygous115262319
121415301814153019GA13GENIChomozygous115262321
121415646714156468AG8GENIChomozygous115363028
121415647814156479CA8GENIChomozygous115262323
121414659814146599AG22GENIChomozygous115437980
121414467614144677CT19GENIChomozygous115437979