chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104289364942893650TC23GENIChomozygous116576996
104289394142893942GA20GENIChomozygous117077334
104289539342895394GA30GENIChomozygous117077335
104289594342895944TC39GENIChomozygous116576998
104289600742896008AG28GENIChomozygous117077336
104289635342896354CT52GENIChomozygous117077337
104289999842899999CT47GENIChomozygous116577004
104290000642900007TC43GENIChomozygous117077339
104290008442900085AG40GENIChomozygous116577006
104290050542900506AG36GENIChomozygous116577008
104290090642900907AG32GENIChomozygous116577010
104290207642902077AG31GENIChomozygous116577014
104290218542902186AC29GENIChomozygous116577016
104290231242902313AG29GENIChomozygous117077340
104290236842902369CA24GENIChomozygous116577018
104291461642914617GT21GENIChomozygous116765910
104291461842914619AT22GENIChomozygous116765912
104291692042916921AC32GENIChomozygous116577030
104291889042918891CA35GENIChomozygous117077341
104292114342921144AG28GENIChomozygous116577036
104292417242924173GA31GENIChomozygous117077342
104292424842924249AG38GENIChomozygous117077343
104292804542928046AT34GENIChomozygous117077345
104292849442928495GA28GENIChomozygous117077346
104292856042928561GT19GENIChomozygous117077347
104292990242929903TC42GENIChomozygous116577048
104293131142931312TC26GENIChomozygous116577054
104293183442931835AG27GENIChomozygous116577056
104293237042932371CA41GENIChomozygous117077350