chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155526136655261367TC23GENIChomozygous48314020
155526140855261409AC12GENIChomozygous48602481
155526141455261415AT13GENIChomozygous48602483
155526143355261434TC9GENIChomozygous48314021
155526144855261449AT13GENIChomozygous48314022
155526170555261706TTATGTC19GENICpossibly homozygous48314024
155526170655261707CA24GENICheterozygous48314025
155526170755261708TTGCTATGGAGGAACCTCA22GENICpossibly homozygous48314026
155526443055264432TG--5GENICheterozygous48314029
155526811455268115GGAA24GENICheterozygous48314031
155526811655268117CG21GENICheterozygous48314032
155526817655268177CG21GENIChomozygous48314033
155526817855268179C-21GENIChomozygous48314034
155527743255277433GT51GENICheterozygous48602487
155527744155277442GT47GENICheterozygous48602489
155527747955277480GT40GENICheterozygous48602491
155527751155277512AT34GENICheterozygous48314045
155527752055277521TA42GENICheterozygous48672025
155527761355277614TA16GENICheterozygous48672027
155527761855277619GA18GENICheterozygous48314049
155527763055277631GT17GENICheterozygous48314050
155527763955277640GT17GENICheterozygous48314051
155526812155268122AC24GENICheterozygous48507246
155526812255268123GT24GENICheterozygous48507248
155527768455277685TG26GENICheterozygous48507252