chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104921088149210882CT10GENICheterozygous51447301
104921128849211289GC27GENIChomozygous51447302
104921192949211930GC17GENICpossibly homozygous51447303
104921329749213298AC17GENIChomozygous51447304
104921335149213352AT21GENICpossibly homozygous51447305
104921437949214380TC19GENICpossibly homozygous51447306
104921487049214871TC12GENIChomozygous51447309
104921650149216502TC24GENIChomozygous51447310
104921735249217353GA16GENIChomozygous51447311
104921889649218897GA15GENICpossibly homozygous51447312
104921925149219252AC3GENIChomozygous51447316
104921949349219494CT28GENICpossibly homozygous51447317
104922011349220114GA7GENICpossibly homozygous51447318
104922066949220670AT18GENICheterozygous51447319
104922096449220966GA--7GENICpossibly homozygous51447320
104922178349221786GGA---7GENICpossibly homozygous51447323
104922216149222162CT10GENICpossibly homozygous51447324
104922240849222409GGA17GENICpossibly homozygous51447325
104922294849222949CT6GENIChomozygous51447326
104922311449223115TA4GENIChomozygous51447327
104922365249223653CCTATT8GENIChomozygous51447328
104922525449225255AT17GENICpossibly homozygous51447329
104922528849225289GA18GENIChomozygous51447330
104922610049226101TC27GENICpossibly homozygous51447331
104922712149227122TA3GENIChomozygous51447332
104922775349227754TC23GENIChomozygous51447333