chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104672938746729388CT53GENIChomozygous51445166
104673366546733671TTAGTC------18GENIChomozygous51445167
104673405646734057GA61GENIChomozygous51445168
104673410846734109GT50GENICpossibly homozygous51445169
104673473246734733CCTT34GENIChomozygous51445170
104673536046735361TC36GENIChomozygous51445171
104673695646736957TA68GENIChomozygous51445172
104673700646737007TC65GENIChomozygous51445173
104673716546737166GA47GENIChomozygous51445174
104673757546737582CACTGCC-------27GENICpossibly homozygous51445175
104673758846737589GT38GENICheterozygous51445176
104673777346737774CT49GENIChomozygous51445177
104673839346738394TC43GENICpossibly homozygous51445178
104673905446739055AG56GENICpossibly homozygous51445179
104673919446739195GT57GENIChomozygous51445180
104673962946739630AG24GENIChomozygous51445181
104673963246739672CTGATTTTCAGGCCACCTCCCCGGCCCAGTCACATAGCTA----------------------------------------5GENIChomozygous51445182
104673970646739707GA49GENIChomozygous51445183
104674013846740139AG35GENIChomozygous51445184
104674029146740292AG28GENIChomozygous51445185
104674030246740303CT30GENIChomozygous51445186
104674082946740830CT41GENIChomozygous51445187
104674122046741221TC46GENIChomozygous51445188
104674160646741607TC52GENIChomozygous51445189
104674188546741886TG49GENIChomozygous51445190
104674211046742111TTGG16GENIChomozygous51445191