chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2122782326122782327CG18GENIChomozygous120145493
2122782727122782728TG24GENICpossibly homozygous120145495
2122783027122783028GA23GENIChomozygous120145496
2122783038122783039GA22GENIChomozygous120145498
2122783115122783116CT18GENIChomozygous120145500
2122783446122783447TA21GENIChomozygous120145502
2122783463122783463A25GENIChomozygous133708823
2122783499122783500TC25GENIChomozygous120145504
2122783591122783592CT17GENIChomozygous120145506
2122783596122783597CT18GENIChomozygous120145507
2122783817122783818CA17GENIChomozygous120145509
2122783857122783858AG18GENIChomozygous110002262
2122784629122784630AG14GENIChomozygous110002265
2122784927122784928TC14GENIChomozygous110002266
2122785078122785079C20GENIChomozygous133708824
2122785086122785087TC20GENIChomozygous110002267
2122785652122785653AG25GENIChomozygous120145511
2122786856122786857TC23GENIChomozygous110002272
2122786869122786870CT21GENIChomozygous110002273
2122788691122788692CT23GENIChomozygous120145512
2122795240122795241AC24GENIChomozygous110002274
2122798250122798251TC28GENIChomozygous110002277
2122800581122800581ATA13GENIChomozygous133708825
2122804607122804608GA15GENIChomozygous120145513