chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409896214098963TA29GENIChomozygous115262269
121409946514099466GA26GENIChomozygous115262271
121410192014101921AG20GENIChomozygous115262273
121410228514102286CT30GENIChomozygous115262275
121410687914106880AG12GENIChomozygous115262277
121413470214134703TG21GENIChomozygous115262283
121413794614137947GT21GENIChomozygous115262285
121413799614137997TC28GENIChomozygous115262287
121412845214128453CA20GENIChomozygous115580714
121414100414141005GA11GENIChomozygous115262289
121414101714141018AG14GENIChomozygous115262291
121414172314141724AT27GENIChomozygous115262293
121414393814143939AG33GENIChomozygous115262295
121414457614144577AC23GENIChomozygous115262297
121414560614145607CT30GENIChomozygous115262299
121414659814146599AG25GENIChomozygous115437980
121414608314146084AC33GENIChomozygous115262301
121414645914146460TC22GENIChomozygous115262303
121414705214147053TC25GENIChomozygous115262305
121414729114147292TC33GENIChomozygous115262307
121414743514147436CT35GENIChomozygous115417741
121414791614147917CT21GENIChomozygous115262309
121414834914148350GT21GENIChomozygous115262311
121414858714148588GT23GENIChomozygous115262313
121414860614148607TC28GENIChomozygous115262315
121414865914148660CT25GENIChomozygous115262317
121414954614149547TA26GENIChomozygous115262319
121415009014150091CT22GENIChomozygous115580716
121415301814153019GA31GENIChomozygous115262321
121415646714156468AG30GENIChomozygous115363028
121415647814156479CA28GENICpossibly homozygous115262323