chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95071414850714149CT24GENIChomozygous117335019
95071490350714904TC133GENICheterozygous117823055
95071491850714919GT120GENICheterozygous117823056
95071492950714930TC109GENICheterozygous117823057
95071592450715925CT55GENICpossibly homozygous117335020
95071667850716679GT36GENICheterozygous117335021
95071668150716682CT40GENICheterozygous117524948
95071690850716909GA33GENIChomozygous117335022
95071926650719267TC54GENICpossibly homozygous117335023
95072523450725235GT57GENIChomozygous117335024
95072644750726448TG37GENIChomozygous117335025
95072960250729603TG22GENIChomozygous117335026
95073049050730491GA51GENIChomozygous117335027
95074042850740429AC43GENICpossibly homozygous117335028
95074050450740505CT59GENIChomozygous117335029
95074052150740522CT64GENIChomozygous117335030
95074073850740739GC51GENIChomozygous117335031
95074178150741782CG48GENICheterozygous117524952
95074179250741793CT46GENICheterozygous117524954
95074182450741825AT53GENICheterozygous117524962
95074193550741936GA51GENICheterozygous117335032
95074217950742180AG54GENICheterozygous117823058
95074220250742203CT47GENICheterozygous117823059
95074220350742204AG48GENICheterozygous117823060
95074319750743198GA49GENICheterozygous117823061
95074391550743916AG36GENIChomozygous117335033
95074464750744648GA55GENICpossibly homozygous117335034