chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409896214098963TA41GENIChomozygous115262269
121409946514099466GA37GENIChomozygous115262271
121410192014101921AG40GENIChomozygous115262273
121410228514102286CT26GENICpossibly homozygous115262275
121410687914106880AG35GENIChomozygous115262277
121413370114133702GC8GENICheterozygous115262279
121413371214133713GT5GENICheterozygous115262281
121413470214134703TG29GENIChomozygous115262283
121413794614137947GT27GENIChomozygous115262285
121413799614137997TC28GENIChomozygous115262287
121414100414141005GA31GENIChomozygous115262289
121414101714141018AG27GENIChomozygous115262291
121414172314141724AT19GENIChomozygous115262293
121414393814143939AG37GENIChomozygous115262295
121414457614144577AC25GENIChomozygous115262297
121414560614145607CT36GENIChomozygous115262299
121414608314146084AC33GENIChomozygous115262301
121414645914146460TC28GENIChomozygous115262303
121414659814146599AG20GENIChomozygous115437980
121413370214133703GC8GENICheterozygous115510032
121414467614144677CT27GENIChomozygous115437979
121414705214147053TC26GENIChomozygous115262305
121414729114147292TC23GENIChomozygous115262307
121414791614147917CT28GENIChomozygous115262309
121414834914148350GT20GENIChomozygous115262311
121414860614148607TC29GENIChomozygous115262315
121414865914148660CT27GENIChomozygous115262317
121414954614149547TA28GENIChomozygous115262319
121415301814153019GA23GENIChomozygous115262321
121415646714156468AG20GENIChomozygous115363028
121415647814156479CA21GENICpossibly homozygous115262323